Code System Concept
Code System Concept Code 276654001
Code System Concept Name Congenital malformation (disorder)
Code System Preferred Concept Name Congenital malformation (disorder)
Concept Status Published
Concept Status Date 09/01/2024
Code System Name SNOMED-CT
Other Relationships
No other relationships present.
Child Concepts

Congenital malformation (disorder) {276654001 , SNOMED-CT }
       Parent/Child (Relationship Type)
[X]Other congenital malformations (disorder) {205973003 , SNOMED-CT } [X]Other specified congenital malformation syndromes, not elsewhere classified (disorder) {205984005 , SNOMED-CT } [X]Other specified congenital malformations (disorder) {205985006 , SNOMED-CT } 11p15 duplication syndrome (disorder) {880079009 , SNOMED-CT } 12q15q21.1 microdeletion syndrome (disorder) {734030009 , SNOMED-CT } 13q partial monosomy syndrome (disorder) {29257000 , SNOMED-CT } 15q11.2 microdeletion syndrome (disorder) {771340007 , SNOMED-CT } 15q11q13 microduplication syndrome (disorder) {719427001 , SNOMED-CT } 15q13.3 microduplication syndrome (disorder) {768713003 , SNOMED-CT } 16p11.2p12.2 microduplication syndrome (disorder) {733518000 , SNOMED-CT } 16p13.11 microduplication syndrome (disorder) {719578005 , SNOMED-CT } 16q24.1 microdeletion syndrome (disorder) {770760006 , SNOMED-CT } 16q24.3 microdeletion syndrome (disorder) {719580004 , SNOMED-CT } 17q11 deletion syndrome (disorder) {880093002 , SNOMED-CT } 17q23.1-q23.2 duplication syndrome (disorder) {890110004 , SNOMED-CT } 17q24-qter duplication syndrome (disorder) {890116005 , SNOMED-CT } 1p21.3 microdeletion syndrome (disorder) {719600006 , SNOMED-CT } 1q21.1 microdeletion syndrome (disorder) {699305004 , SNOMED-CT } 20p12.2 deletion syndrome (disorder) {890117001 , SNOMED-CT } 22q11.2 duplication syndrome (disorder) {699311001 , SNOMED-CT } 22q13.3 deletion syndrome (disorder) {699310000 , SNOMED-CT } 2q24 microdeletion syndrome (disorder) {719658006 , SNOMED-CT } 3p25.3 deletion syndrome (disorder) {890123006 , SNOMED-CT } 5q22.2 deletion syndrome (disorder) {890124000 , SNOMED-CT } 7p partial monosomy (disorder) {24786004 , SNOMED-CT } 7p12-p14 deletion syndrome (disorder) {890125004 , SNOMED-CT } 7p21.1 deletion syndrome (disorder) {890127007 , SNOMED-CT } 7q31 microdeletion syndrome (disorder) {773326003 , SNOMED-CT } 9p24.3 deletion syndrome (disorder) {890128002 , SNOMED-CT } 9q34 deletion syndrome (disorder) {890130000 , SNOMED-CT } Abdominal heart (disorder) {14886009 , SNOMED-CT } Aberrant insertion of frenum of tongue (disorder) {109556002 , SNOMED-CT } Aberrant insertion of labial frenulum (disorder) {109551007 , SNOMED-CT } Aberrant muscle of the lower limb (disorder) {205365003 , SNOMED-CT } Aberrant muscle of the upper limb (disorder) {253916007 , SNOMED-CT } Aberrant parathyroid gland (disorder) {205757003 , SNOMED-CT } Aberrant thyroid gland (disorder) {268302006 , SNOMED-CT } Ablepharon (disorder) {13401001 , SNOMED-CT } Abnormal communication between pericardial sac and peritoneal cavity (disorder) {91841003 , SNOMED-CT } Abnormal fetal duplication (disorder) {72014004 , SNOMED-CT } Abnormality of right atrioventricular valve in double inlet ventricle (disorder) {253454000 , SNOMED-CT } Absence of septum pellucidum (disorder) {253143001 , SNOMED-CT } Absence of the vermis (disorder) {253177006 , SNOMED-CT } Acardia (disorder) {205834002 , SNOMED-CT } Acardius (disorder) {84648007 , SNOMED-CT } Accessory adrenal gland (disorder) {68352004 , SNOMED-CT } Accessory breast (disorder) {18166000 , SNOMED-CT } Accessory broad ligament (disorder) {21565000 , SNOMED-CT } Accessory carpal bones (disorder) {20136007 , SNOMED-CT } Accessory eyelid (disorder) {24606006 , SNOMED-CT } Accessory fallopian tube (disorder) {48672005 , SNOMED-CT } Accessory hepatic duct (disorder) {78560000 , SNOMED-CT } Accessory kidney (disorder) {30275001 , SNOMED-CT } Accessory lacrimal canal (disorder) {53697002 , SNOMED-CT } Accessory lacrimal gland disorder (disorder) {58670006 , SNOMED-CT } Accessory liver (disorder) {71728002 , SNOMED-CT } Accessory nose (disorder) {1856001 , SNOMED-CT } Accessory ossification center (disorder) {63413008 , SNOMED-CT } Accessory ovary (disorder) {37975005 , SNOMED-CT } Accessory pancreas (disorder) {79037006 , SNOMED-CT } Accessory parathyroid gland (disorder) {65048006 , SNOMED-CT } Accessory pituitary gland (disorder) {205750001 , SNOMED-CT } Accessory rib (disorder) {205460009 , SNOMED-CT } Accessory skeletal muscle (disorder) {50847000 , SNOMED-CT } Accessory spleen (disorder) {10362008 , SNOMED-CT } Accessory sternebral ossification site (disorder) {91847004 , SNOMED-CT } Accessory thymic tissue (disorder) {24358005 , SNOMED-CT } Accessory thyroid gland (disorder) {65237009 , SNOMED-CT } Accessory tissue on tricuspid leaflet (disorder) {253384009 , SNOMED-CT } Accessory tragus (disorder) {204245004 , SNOMED-CT } Accessory tragus of ear (disorder) {29435005 , SNOMED-CT } Accessory ureter (disorder) {64727007 , SNOMED-CT } Accessory urethra (disorder) {82635007 , SNOMED-CT } Accessory urinary bladder (disorder) {62500006 , SNOMED-CT } Acephalocheiria (disorder) {63340009 , SNOMED-CT } Acephalorhachia (disorder) {7727004 , SNOMED-CT } Acephalothorax (disorder) {205837009 , SNOMED-CT } Acephaly (disorder) {91848009 , SNOMED-CT } Acraniate monster (disorder) {36745003 , SNOMED-CT } Adactyly (disorder) {275348004 , SNOMED-CT } Additional sex chromosome (disorder) {205705003 , SNOMED-CT } Aganglionosis of parasympathetic nerve ganglia (disorder) {64370005 , SNOMED-CT } Agenesis of cerebellum (disorder) {253172000 , SNOMED-CT } Agenesis of cerebrum (disorder) {204040004 , SNOMED-CT } Agenesis of corpus callosum (disorder) {5102002 , SNOMED-CT } Agenesis of eye (disorder) {204099004 , SNOMED-CT } Agenesis of nerve (disorder) {111338006 , SNOMED-CT } Agenesis of punctum lacrimale (disorder) {204208005 , SNOMED-CT } Albinism (disorder) {15890002 , SNOMED-CT } Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) {734349003 , SNOMED-CT } Amegakaryocytic thrombocytopenia with congenital malformation (disorder) {359531004 , SNOMED-CT } Amelogenesis imperfecta (disorder) {78494001 , SNOMED-CT } Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism (disorder) {109472008 , SNOMED-CT } Amyelencephalus (disorder) {75076004 , SNOMED-CT } Amyelia (disorder) {78784005 , SNOMED-CT } Amyotrophia congenita (disorder) {75491005 , SNOMED-CT } Anal atresia (disorder) {204712000 , SNOMED-CT } Anodontia (disorder) {26624006 , SNOMED-CT } Anomalies of lens shape (disorder) {204132007 , SNOMED-CT } Anonychia (disorder) {23610003 , SNOMED-CT } Anophthalmos (disorder) {7183006 , SNOMED-CT } Anorectal agenesis (disorder) {975000 , SNOMED-CT } Aplasia cutis congenita (disorder) {35484002 , SNOMED-CT } Arnold-Chiari syndrome (disorder) {27905003 , SNOMED-CT } Arterial malformation (disorder) {234119001 , SNOMED-CT } Atresia of foramen of Luschka (disorder) {61292006 , SNOMED-CT } Atresia of foramen of Magendie (disorder) {30299001 , SNOMED-CT } Atresia of large intestine (disorder) {204711007 , SNOMED-CT } Atresia of nasolacrimal duct (disorder) {278530008 , SNOMED-CT } Atresia of pupil (disorder) {17480001 , SNOMED-CT } Atresia of urinary meatus (disorder) {79788002 , SNOMED-CT } Atrioventricular septal defect and common atrioventricular junction (disorder) {253414002 , SNOMED-CT } Bicuspid cardiac valve (disorder) {76257003 , SNOMED-CT } Bifid nail (disorder) {110992006 , SNOMED-CT } Bifid patella (disorder) {79214007 , SNOMED-CT } Bifid thumb (disorder) {51219000 , SNOMED-CT } Bifid tongue (disorder) {84557007 , SNOMED-CT } Bone island (disorder) {25994006 , SNOMED-CT } Bowen-Conradi syndrome (disorder) {711153001 , SNOMED-CT } Branchial cleft anomaly (disorder) {362998000 , SNOMED-CT } Byzanthine arch palate (disorder) {27272007 , SNOMED-CT } Cat eye syndrome (disorder) {26445008 , SNOMED-CT } Cavernous lymphangioma of skin (disorder) {254793001 , SNOMED-CT } Celoschisis (disorder) {71468002 , SNOMED-CT } Central nervous system malformation in fetus affecting obstetrical care (disorder) {1538006 , SNOMED-CT } Cerebellar cortical dysplasia (disorder) {253179009 , SNOMED-CT } Cerebellar hemangioblastomatosis (disorder) {74073002 , SNOMED-CT } Cervical auricle (disorder) {26885007 , SNOMED-CT } Cervical rib (disorder) {72535009 , SNOMED-CT } Cervical spinal hydromeningocele (disorder) {203969004 , SNOMED-CT } Chiari malformation (disorder) {253184003 , SNOMED-CT } Chondrodystrophy malacia (disorder) {84176000 , SNOMED-CT } Chromosome 16p11.2 deletion syndrome (disorder) {699307007 , SNOMED-CT } Chromosome 1p36 deletion syndrome (disorder) {699306003 , SNOMED-CT } Chromosome 2q37 deletion syndrome (disorder) {702357000 , SNOMED-CT } Chromosome Xp11.3 microdeletion syndrome (disorder) {719808002 , SNOMED-CT } Cleft cartilaginous centrum of cervical vertebra (disorder) {92489003 , SNOMED-CT } Cleft cartilaginous centrum of lumbar vertebra (disorder) {92490007 , SNOMED-CT } Cleft cartilaginous centrum of sacral vertebra (disorder) {92491006 , SNOMED-CT } Cleft cartilaginous centrum of thoracic vertebra (disorder) {92492004 , SNOMED-CT } Cleft face (disorder) {92821006 , SNOMED-CT } Cleft lip (disorder) {80281008 , SNOMED-CT } Cleft palate (disorder) {87979003 , SNOMED-CT } Cleft tongue (disorder) {204630003 , SNOMED-CT } Coloboma of eyelid (disorder) {95202004 , SNOMED-CT } Commissural fusion of truncal valve (disorder) {449139001 , SNOMED-CT } Common atrioventricular orifice in double inlet ventricle (disorder) {445294008 , SNOMED-CT } Complete aphalangia of lower limb (disorder) {89434002 , SNOMED-CT } Complete trisomy 16 syndrome (disorder) {77269002 , SNOMED-CT } Complete trisomy 18 syndrome (disorder) {51500006 , SNOMED-CT } Complete trisomy 20 syndrome (disorder) {53346000 , SNOMED-CT } Complete trisomy 21 syndrome (disorder) {41040004 , SNOMED-CT } Complete trisomy 22 syndrome (disorder) {71703005 , SNOMED-CT } Congenital abnormal fusion of adrenal glands (disorder) {92833001 , SNOMED-CT } Congenital abnormal fusion of alisphenoid bone (disorder) {92834007 , SNOMED-CT } Congenital abnormal fusion of arch of caudal vertebra (disorder) {92835008 , SNOMED-CT } Congenital abnormal fusion of arch of cervical vertebra (disorder) {92836009 , SNOMED-CT } Congenital abnormal fusion of arch of lumbar vertebra (disorder) {92837000 , SNOMED-CT } Congenital abnormal fusion of arch of sacral vertebra (disorder) {92838005 , SNOMED-CT } Congenital abnormal fusion of arch of thoracic vertebra (disorder) {92839002 , SNOMED-CT } Congenital abnormal fusion of basioccipital bone (disorder) {92840000 , SNOMED-CT } Congenital abnormal fusion of basisphenoid bone (disorder) {92841001 , SNOMED-CT } Congenital abnormal fusion of carpal bone (disorder) {92843003 , SNOMED-CT } Congenital abnormal fusion of centrum of caudal vertebra (disorder) {92848007 , SNOMED-CT } Congenital abnormal fusion of centrum of cervical vertebra (disorder) {92849004 , SNOMED-CT } Congenital abnormal fusion of centrum of lumbar vertebra (disorder) {92850004 , SNOMED-CT } Congenital abnormal fusion of centrum of sacral vertebra (disorder) {92851000 , SNOMED-CT } Congenital abnormal fusion of centrum of thoracic vertebra (disorder) {92852007 , SNOMED-CT } Congenital abnormal fusion of exoccipital bone (disorder) {92853002 , SNOMED-CT } Congenital abnormal fusion of fibula (disorder) {92855009 , SNOMED-CT } Congenital abnormal fusion of frontal bone (disorder) {92857001 , SNOMED-CT } Congenital abnormal fusion of humerus (disorder) {92859003 , SNOMED-CT } Congenital abnormal fusion of ilium (disorder) {92860008 , SNOMED-CT } Congenital abnormal fusion of interparietal bone (disorder) {92861007 , SNOMED-CT } Congenital abnormal fusion of ischium (disorder) {92862000 , SNOMED-CT } Congenital abnormal fusion of lacrimal bone (disorder) {92863005 , SNOMED-CT } Congenital abnormal fusion of liver lobes (disorder) {92864004 , SNOMED-CT } Congenital abnormal fusion of mandible (disorder) {92865003 , SNOMED-CT } Congenital abnormal fusion of maxilla (disorder) {92866002 , SNOMED-CT } Congenital abnormal fusion of metacarpal bone (disorder) {92867006 , SNOMED-CT } Congenital abnormal fusion of metatarsal bone (disorder) {92868001 , SNOMED-CT } Congenital abnormal fusion of nasal bone (disorder) {92869009 , SNOMED-CT } Congenital abnormal fusion of palatine bone (disorder) {92870005 , SNOMED-CT } Congenital abnormal fusion of parietal bone (disorder) {92871009 , SNOMED-CT } Congenital abnormal fusion of premaxilla (disorder) {92872002 , SNOMED-CT } Congenital abnormal fusion of presphenoid bone (disorder) {92873007 , SNOMED-CT } Congenital abnormal fusion of radius (disorder) {92874001 , SNOMED-CT } Congenital abnormal fusion of squamosal bone (disorder) {92876004 , SNOMED-CT } Congenital abnormal fusion of supraoccipital bone (disorder) {92877008 , SNOMED-CT } Congenital abnormal fusion of tarsal bone (disorder) {92879006 , SNOMED-CT } Congenital abnormal fusion of tympanic anulus (disorder) {92881008 , SNOMED-CT } Congenital abnormal fusion of ulna (disorder) {92882001 , SNOMED-CT } Congenital abnormal fusion of zygomatic bone (disorder) {92884000 , SNOMED-CT } Congenital abnormal shape of adrenal gland (disorder) {92886003 , SNOMED-CT } Congenital abnormal shape of alisphenoid bone (disorder) {92887007 , SNOMED-CT } Congenital abnormal shape of aortic valve (disorder) {92888002 , SNOMED-CT } Congenital abnormal shape of arch of caudal vertebra (disorder) {92889005 , SNOMED-CT } Congenital abnormal shape of arch of cervical vertebra (disorder) {92890001 , SNOMED-CT } Congenital abnormal shape of arch of lumbar vertebra (disorder) {92891002 , SNOMED-CT } Congenital abnormal shape of arch of sacral vertebra (disorder) {92892009 , SNOMED-CT } Congenital abnormal shape of arch of thoracic vertebra (disorder) {92893004 , SNOMED-CT } Congenital abnormal shape of auditory ossicles (disorder) {92894005 , SNOMED-CT } Congenital abnormal shape of basioccipital bone (disorder) {92895006 , SNOMED-CT } Congenital abnormal shape of basisphenoid bone (disorder) {92896007 , SNOMED-CT } Congenital abnormal shape of carpal bone (disorder) {92898008 , SNOMED-CT } Congenital abnormal shape of centrum of caudal vertebra (disorder) {92899000 , SNOMED-CT } Congenital abnormal shape of centrum of cervical vertebra (disorder) {92900005 , SNOMED-CT } Congenital abnormal shape of centrum of lumbar vertebra (disorder) {92901009 , SNOMED-CT } Congenital abnormal shape of centrum of sacral vertebra (disorder) {92902002 , SNOMED-CT } Congenital abnormal shape of centrum of thoracic vertebra (disorder) {92903007 , SNOMED-CT } Congenital abnormal shape of cerebellum (disorder) {92904001 , SNOMED-CT } Congenital abnormal shape of cerebrum (disorder) {92905000 , SNOMED-CT } Congenital abnormal shape of clavicle (disorder) {92906004 , SNOMED-CT } Congenital abnormal shape of digit (disorder) {92907008 , SNOMED-CT } Congenital abnormal shape of exoccipital bone (disorder) {92908003 , SNOMED-CT } Congenital abnormal shape of fallopian tube (disorder) {92933000 , SNOMED-CT } Congenital abnormal shape of femur (disorder) {92909006 , SNOMED-CT } Congenital abnormal shape of fibula (disorder) {92910001 , SNOMED-CT } Congenital abnormal shape of frontal bone (disorder) {92912009 , SNOMED-CT } Congenital abnormal shape of gallbladder (disorder) {92913004 , SNOMED-CT } Congenital abnormal shape of humerus (disorder) {92915006 , SNOMED-CT } Congenital abnormal shape of hyoid bone (disorder) {92916007 , SNOMED-CT } Congenital abnormal shape of ilium (disorder) {92917003 , SNOMED-CT } Congenital abnormal shape of inner ear (disorder) {92918008 , SNOMED-CT } Congenital abnormal shape of interparietal bone (disorder) {92919000 , SNOMED-CT } Congenital abnormal shape of ischium (disorder) {92920006 , SNOMED-CT } Congenital abnormal shape of kidney (disorder) {92921005 , SNOMED-CT } Congenital abnormal shape of lacrimal bone (disorder) {92922003 , SNOMED-CT } Congenital abnormal shape of liver (disorder) {92924002 , SNOMED-CT } Congenital abnormal shape of mandible (disorder) {92926000 , SNOMED-CT } Congenital abnormal shape of maxilla (disorder) {92927009 , SNOMED-CT } Congenital abnormal shape of metacarpal bone (disorder) {92928004 , SNOMED-CT } Congenital abnormal shape of metatarsal bone (disorder) {92929007 , SNOMED-CT } Congenital abnormal shape of mitral valve (disorder) {92923008 , SNOMED-CT } Congenital abnormal shape of nasal bone (disorder) {92930002 , SNOMED-CT } Congenital abnormal shape of ovary (disorder) {92932005 , SNOMED-CT } Congenital abnormal shape of palate rugae (disorder) {92934006 , SNOMED-CT } Congenital abnormal shape of palatine bone (disorder) {92935007 , SNOMED-CT } Congenital abnormal shape of parietal bone (disorder) {92936008 , SNOMED-CT } Congenital abnormal shape of pinna (disorder) {92937004 , SNOMED-CT } Congenital abnormal shape of premaxilla (disorder) {92938009 , SNOMED-CT } Congenital abnormal shape of presphenoid bone (disorder) {92939001 , SNOMED-CT } Congenital abnormal shape of pubis (disorder) {92940004 , SNOMED-CT } Congenital abnormal shape of pulmonary valve (disorder) {92941000 , SNOMED-CT } Congenital abnormal shape of radius (disorder) {92942007 , SNOMED-CT } Congenital abnormal shape of rib (disorder) {92943002 , SNOMED-CT } Congenital abnormal shape of scapula (disorder) {92945009 , SNOMED-CT } Congenital abnormal shape of spleen (disorder) {92946005 , SNOMED-CT } Congenital abnormal shape of squamosal bone (disorder) {92947001 , SNOMED-CT } Congenital abnormal shape of sternebra (disorder) {92948006 , SNOMED-CT } Congenital abnormal shape of supraoccipital bone (disorder) {92949003 , SNOMED-CT } Congenital abnormal shape of tarsal bone (disorder) {92951004 , SNOMED-CT } Congenital abnormal shape of testis (disorder) {92952006 , SNOMED-CT } Congenital abnormal shape of thymus (disorder) {92953001 , SNOMED-CT } Congenital abnormal shape of tibia (disorder) {92954007 , SNOMED-CT } Congenital abnormal shape of tricuspid valve (disorder) {92944008 , SNOMED-CT } Congenital abnormal shape of tympanic anulus (disorder) {92955008 , SNOMED-CT } Congenital abnormal shape of ulna (disorder) {92956009 , SNOMED-CT } Congenital abnormal shape of uterus (disorder) {92957000 , SNOMED-CT } Congenital abnormal shape of zygomatic bone (disorder) {92959002 , SNOMED-CT } Congenital abnormality of lower limb and pelvic girdle (disorder) {253937004 , SNOMED-CT } Congenital abnormality of oral cavity (disorder) {282041002 , SNOMED-CT } Congenital absence (disorder) {702626005 , SNOMED-CT } Congenital absence of adrenal gland (disorder) {83190008 , SNOMED-CT } Congenital absence of alimentary tract (disorder) {66793004 , SNOMED-CT } Congenital absence of all toes (disorder) {37221009 , SNOMED-CT } Congenital absence of auricle with atresia of auditory canal (disorder) {38919006 , SNOMED-CT } Congenital absence of bile duct (disorder) {1287007 , SNOMED-CT } Congenital absence of breast (disorder) {111324004 , SNOMED-CT } Congenital absence of broad ligament (disorder) {24787008 , SNOMED-CT } Congenital absence of cervix (disorder) {37687000 , SNOMED-CT } Congenital absence of chin (disorder) {204285005 , SNOMED-CT } Congenital absence of claw (disorder) {91881005 , SNOMED-CT } Congenital absence of clitoris (disorder) {60291005 , SNOMED-CT } Congenital absence of ear (disorder) {71619006 , SNOMED-CT } Congenital absence of epididymis (disorder) {91882003 , SNOMED-CT } Congenital absence of eye bulge (disorder) {92966001 , SNOMED-CT } Congenital absence of eyelash (disorder) {63935007 , SNOMED-CT } Congenital absence of finger (disorder) {48301005 , SNOMED-CT } Congenital absence of foot (disorder) {371197005 , SNOMED-CT } Congenital absence of gallbladder (disorder) {86507001 , SNOMED-CT } Congenital absence of genital tubercle (disorder) {92967005 , SNOMED-CT } Congenital absence of heart structure (disorder) {413905004 , SNOMED-CT } Congenital absence of jaw (disorder) {91922000 , SNOMED-CT } Congenital absence of lacrimal apparatus (disorder) {7929009 , SNOMED-CT } Congenital absence of lacrimal drainage structure (disorder) {418087009 , SNOMED-CT } Congenital absence of leg with foot AND toes (disorder) {17021009 , SNOMED-CT } Congenital absence of liver (disorder) {3650004 , SNOMED-CT } Congenital absence of muscle AND/OR tendon (disorder) {47880003 , SNOMED-CT } Congenital absence of nose (disorder) {111317000 , SNOMED-CT } Congenital absence of ovary (disorder) {12017008 , SNOMED-CT } Congenital absence of oviduct (disorder) {92973006 , SNOMED-CT } Congenital absence of parathyroid gland (disorder) {73291005 , SNOMED-CT } Congenital absence of part of brain (disorder) {26595007 , SNOMED-CT } Congenital absence of paw (disorder) {91942009 , SNOMED-CT } Congenital absence of penis (disorder) {59981001 , SNOMED-CT } Congenital absence of pituitary gland (disorder) {205749001 , SNOMED-CT } Congenital absence of prostate (disorder) {51693009 , SNOMED-CT } Congenital absence of renal papilla (disorder) {92975004 , SNOMED-CT } Congenital absence of skeletal bone (disorder) {127328006 , SNOMED-CT } Congenital absence of skeletal muscle (disorder) {38776003 , SNOMED-CT } Congenital absence of spermatic cord (disorder) {88656003 , SNOMED-CT } Congenital absence of spine (disorder) {254038003 , SNOMED-CT } Congenital absence of spleen (disorder) {93030006 , SNOMED-CT } Congenital absence of tail (disorder) {91912006 , SNOMED-CT } Congenital absence of tendon (disorder) {271018002 , SNOMED-CT } Congenital absence of testis (disorder) {274151005 , SNOMED-CT } Congenital absence of thymus (disorder) {91918005 , SNOMED-CT } Congenital absence of thyroid gland (disorder) {92978002 , SNOMED-CT } Congenital absence of toe (disorder) {66345008 , SNOMED-CT } Congenital absence of ureter (disorder) {77761000 , SNOMED-CT } Congenital absence of urethra (disorder) {1922008 , SNOMED-CT } Congenital absence of urinary bladder (disorder) {22421007 , SNOMED-CT } Congenital absence of uterus (disorder) {17142008 , SNOMED-CT } Congenital absence of vagina (disorder) {87380008 , SNOMED-CT } Congenital absence of vein (disorder) {40627003 , SNOMED-CT } Congenital absence of vulva (disorder) {111335009 , SNOMED-CT } Congenital adhesions of cerebral meninges (disorder) {204072001 , SNOMED-CT } Congenital adhesions of omentum (disorder) {57921006 , SNOMED-CT } Congenital adhesions of peritoneum (disorder) {29642000 , SNOMED-CT } Congenital adhesions of tongue (disorder) {703000 , SNOMED-CT } Congenital aganglionic megacolon (disorder) {204739008 , SNOMED-CT } Congenital agenesis of brainstem nuclei (disorder) {307359001 , SNOMED-CT } Congenital alopecia (disorder) {2965006 , SNOMED-CT } Congenital aneurysm of heart (disorder) {204395001 , SNOMED-CT } Congenital aniridia (disorder) {69278003 , SNOMED-CT } Congenital ankylosis of elbow (disorder) {86818009 , SNOMED-CT } Congenital anomaly of back (disorder) {363025000 , SNOMED-CT } Congenital anomaly of body cavity (disorder) {363026004 , SNOMED-CT } Congenital anomaly of body wall (disorder) {363027008 , SNOMED-CT } Congenital anomaly of cardiovascular system (disorder) {9904008 , SNOMED-CT } Congenital anomaly of craniovertebral junction (disorder) {88721000119100 , SNOMED-CT } Congenital anomaly of digestive system (disorder) {69518005 , SNOMED-CT } Congenital anomaly of endocrine gland (disorder) {4184009 , SNOMED-CT } Congenital anomaly of fetus (disorder) {702709008 , SNOMED-CT } Congenital anomaly of head (disorder) {87290003 , SNOMED-CT } Congenital anomaly of integument (disorder) {38164009 , SNOMED-CT } Congenital anomaly of lacrimal gland (disorder) {41620007 , SNOMED-CT } Congenital anomaly of lens shape (disorder) {33521009 , SNOMED-CT } Congenital anomaly of limb (disorder) {60475009 , SNOMED-CT } Congenital anomaly of mother complicating pregnancy (disorder) {721153000 , SNOMED-CT } Congenital anomaly of musculoskeletal system (disorder) {73573004 , SNOMED-CT } Congenital anomaly of neck (disorder) {40052002 , SNOMED-CT } Congenital anomaly of nervous system (disorder) {88425004 , SNOMED-CT } Congenital anomaly of nose (disorder) {128274005 , SNOMED-CT } Congenital anomaly of palate (disorder) {128336000 , SNOMED-CT } Congenital anomaly of sternebra (disorder) {93025007 , SNOMED-CT } Congenital anomaly of the hematopoietic system (disorder) {40888008 , SNOMED-CT } Congenital anomaly of trunk (disorder) {78626001 , SNOMED-CT } Congenital anomaly of visual system (disorder) {127329003 , SNOMED-CT } Congenital aphakia (disorder) {35387008 , SNOMED-CT } Congenital asymmetry of jaw (disorder) {90693008 , SNOMED-CT } Congenital atresia of aortic valve (disorder) {51442005 , SNOMED-CT } Congenital atresia of broad ligament (disorder) {79977000 , SNOMED-CT } Congenital atresia of cardiac valve (disorder) {123656005 , SNOMED-CT } Congenital atresia of ejaculatory duct (disorder) {29345006 , SNOMED-CT } Congenital atresia of esophagus (disorder) {26179002 , SNOMED-CT } Congenital atresia of external auditory canal (disorder) {75355004 , SNOMED-CT } Congenital atresia of fallopian tube (disorder) {42618007 , SNOMED-CT } Congenital atresia of intestinal tract (disorder) {93032003 , SNOMED-CT } Congenital atresia of mitral valve (disorder) {23063005 , SNOMED-CT } Congenital atresia of osseous meatus of middle ear (disorder) {43063000 , SNOMED-CT } Congenital atresia of pulmonary valve (disorder) {52670000 , SNOMED-CT } Congenital atresia of pulmonary valve (disorder) {204342004 , SNOMED-CT } Congenital atresia of tricuspid valve (disorder) {63042009 , SNOMED-CT } Congenital atresia of ureter (disorder) {49534003 , SNOMED-CT } Congenital atresia of uterus (disorder) {93034002 , SNOMED-CT } Congenital atresia of vas deferens (disorder) {39513007 , SNOMED-CT } Congenital atresia of vein (disorder) {81103005 , SNOMED-CT } Congenital bent tail (disorder) {92990000 , SNOMED-CT } Congenital biliary atresia (disorder) {77480004 , SNOMED-CT } Congenital bony fusion of phalanges (disorder) {373427001 , SNOMED-CT } Congenital bowing of tibia and/or fibula (disorder) {9252005 , SNOMED-CT } Congenital bronchoesophageal fistula without atresia (disorder) {302949004 , SNOMED-CT } Congenital cerebral cyst (disorder) {19276002 , SNOMED-CT } Congenital cerebral meningocele (disorder) {36010004 , SNOMED-CT } Congenital cervicoaural fistula (disorder) {66597000 , SNOMED-CT } Congenital chordee (disorder) {64320007 , SNOMED-CT } Congenital cleft hand (disorder) {13624003 , SNOMED-CT } Congenital cleft of cardiac valve (disorder) {123658006 , SNOMED-CT } Congenital cleft of thymus (disorder) {92501000 , SNOMED-CT } Congenital coloboma of optic disc (disorder) {44295002 , SNOMED-CT } Congenital complete absence of limb (disorder) {62588002 , SNOMED-CT } Congenital cystic eyeball (disorder) {58882000 , SNOMED-CT } Congenital deformity (disorder) {276655000 , SNOMED-CT } Congenital dermal sinus (disorder) {70499005 , SNOMED-CT } Congenital diaphragmatic hernia (disorder) {17190001 , SNOMED-CT } Congenital dilatation of aortic arch (disorder) {93050005 , SNOMED-CT } Congenital dilatation of atrium (disorder) {93051009 , SNOMED-CT } Congenital dilatation of cardiac ventricle (disorder) {93053007 , SNOMED-CT } Congenital dilatation of colon (disorder) {24291004 , SNOMED-CT } Congenital dilatation of esophagus (disorder) {3004001 , SNOMED-CT } Congenital dilatation of inferior vena cava (disorder) {93056004 , SNOMED-CT } Congenital dilatation of intestinal tract (disorder) {93058003 , SNOMED-CT } Congenital dilatation of lobar intrahepatic bile duct (disorder) {111331000 , SNOMED-CT } Congenital dilatation of stomach (disorder) {93060001 , SNOMED-CT } Congenital dilatation of superior vena cava (disorder) {93062009 , SNOMED-CT } Congenital dilatation of urinary bladder (disorder) {93052002 , SNOMED-CT } Congenital dilation of bile duct (disorder) {204797007 , SNOMED-CT } Congenital dislocation of knee with genu recurvatum (disorder) {15453007 , SNOMED-CT } Congenital diverticulum of bile duct (disorder) {204798002 , SNOMED-CT } Congenital diverticulum of intestinal tract (disorder) {93063004 , SNOMED-CT } Congenital diverticulum of lacrimal canaliculus (disorder) {95507006 , SNOMED-CT } Congenital diverticulum of left ventricle (disorder) {75270000 , SNOMED-CT } Congenital diverticulum of stomach (disorder) {90669003 , SNOMED-CT } Congenital diverticulum of urinary bladder (disorder) {81107006 , SNOMED-CT } Congenital double-tipped tail (disorder) {93065006 , SNOMED-CT } Congenital duplication of cervix (disorder) {58135005 , SNOMED-CT } Congenital duplication of digestive organs (disorder) {33257003 , SNOMED-CT } Congenital duplication of uterus (disorder) {15545001 , SNOMED-CT } Congenital duplication of vagina (disorder) {34424009 , SNOMED-CT } Congenital ectodermal defect (disorder) {254154003 , SNOMED-CT } Congenital ectopic lens (disorder) {74969002 , SNOMED-CT } Congenital ectopic pupil (disorder) {392461003 , SNOMED-CT } Congenital elephantiasis (disorder) {205545009 , SNOMED-CT } Congenital elliptocytosis (disorder) {178935009 , SNOMED-CT } Congenital enlargement of nasopharynx (disorder) {50267003 , SNOMED-CT } Congenital esophageal fistula (disorder) {204652007 , SNOMED-CT } Congenital esophagobronchial fistula (disorder) {41279003 , SNOMED-CT } Congenital eventration of diaphragm (disorder) {17128000 , SNOMED-CT } Congenital exomphalos (disorder) {5867007 , SNOMED-CT } Congenital exophthalmos (disorder) {93081001 , SNOMED-CT } Congenital failure of fusion between maxillary and mandibular processes (disorder) {413906003 , SNOMED-CT } Congenital fenestration of alisphenoid bone (disorder) {92980008 , SNOMED-CT } Congenital fenestration of basioccipital bone (disorder) {93035001 , SNOMED-CT } Congenital fenestration of basisphenoid bone (disorder) {93036000 , SNOMED-CT } Congenital fenestration of exoccipital bone (disorder) {93080000 , SNOMED-CT } Congenital fenestration of frontal bone (disorder) {93082008 , SNOMED-CT } Congenital fenestration of interparietal bone (disorder) {93083003 , SNOMED-CT } Congenital fenestration of nasal bone (disorder) {93084009 , SNOMED-CT } Congenital fenestration of parietal bone (disorder) {93085005 , SNOMED-CT } Congenital fenestration of premaxilla (disorder) {93086006 , SNOMED-CT } Congenital fenestration of presphenoid bone (disorder) {93087002 , SNOMED-CT } Congenital fenestration of squamosal bone (disorder) {93088007 , SNOMED-CT } Congenital fenestration of supraoccipital bone (disorder) {93089004 , SNOMED-CT } Congenital fissure of sternum (disorder) {25642007 , SNOMED-CT } Congenital fistula of anus (disorder) {253774006 , SNOMED-CT } Congenital fistula of auricle (disorder) {111340001 , SNOMED-CT } Congenital fistula of intestinal tract (disorder) {93091007 , SNOMED-CT } Congenital fistula of rectum and anus (disorder) {302952007 , SNOMED-CT } Congenital fistula of urachus (disorder) {50986000 , SNOMED-CT } Congenital fleshy tail tab (disorder) {93092000 , SNOMED-CT } Congenital fold of posterior segment of eye (disorder) {65997000 , SNOMED-CT } Congenital fusion of kidneys (disorder) {42108003 , SNOMED-CT } Congenital fusion of ossicles of ear (disorder) {54386000 , SNOMED-CT } Congenital fusion of pulmonic cusps (disorder) {204345002 , SNOMED-CT } Congenital fusion of ribs (disorder) {66102006 , SNOMED-CT } Congenital fusion of spine (disorder) {38827001 , SNOMED-CT } Congenital fusion of testis (disorder) {44964000 , SNOMED-CT } Congenital gastric perforation (disorder) {53076002 , SNOMED-CT } Congenital gastrointestinal-urinary tract fistula (disorder) {253909006 , SNOMED-CT } Congenital hamartoma (disorder) {399960008 , SNOMED-CT } Congenital hemihypertrophy (disorder) {205838004 , SNOMED-CT } Congenital hereditary endothelial dystrophy (disorder) {417651000 , SNOMED-CT } Congenital hernia of bladder (disorder) {28084002 , SNOMED-CT } Congenital hernia of urinary bladder (disorder) {205022009 , SNOMED-CT } Congenital hiatus hernia (disorder) {47028006 , SNOMED-CT } Congenital hydroureter (disorder) {31290005 , SNOMED-CT } Congenital hypoplasia of adrenal gland (disorder) {93235007 , SNOMED-CT } Congenital hypoplasia of alisphenoid bone (disorder) {93236008 , SNOMED-CT } Congenital hypoplasia of arch of caudal vertebra (disorder) {93238009 , SNOMED-CT } Congenital hypoplasia of arch of cervical vertebra (disorder) {93239001 , SNOMED-CT } Congenital hypoplasia of arch of lumbar vertebra (disorder) {93240004 , SNOMED-CT } Congenital hypoplasia of arch of sacral vertebra (disorder) {93241000 , SNOMED-CT } Congenital hypoplasia of arch of thoracic vertebra (disorder) {93242007 , SNOMED-CT } Congenital hypoplasia of basioccipital bone (disorder) {93243002 , SNOMED-CT } Congenital hypoplasia of basisphenoid bone (disorder) {93244008 , SNOMED-CT } Congenital hypoplasia of bile duct (disorder) {68094008 , SNOMED-CT } Congenital hypoplasia of brain (disorder) {127551000119100 , SNOMED-CT } Congenital hypoplasia of breast (disorder) {8915006 , SNOMED-CT } Congenital hypoplasia of carpal bone (disorder) {93248006 , SNOMED-CT } Congenital hypoplasia of choroid (disorder) {95491001 , SNOMED-CT } Congenital hypoplasia of clavicle (disorder) {93250003 , SNOMED-CT } Congenital hypoplasia of claw (disorder) {93251004 , SNOMED-CT } Congenital hypoplasia of exoccipital bone (disorder) {93253001 , SNOMED-CT } Congenital hypoplasia of eye bulge (disorder) {93254007 , SNOMED-CT } Congenital hypoplasia of fallopian tube (disorder) {93280008 , SNOMED-CT } Congenital hypoplasia of femur (disorder) {93255008 , SNOMED-CT } Congenital hypoplasia of fibula (disorder) {93256009 , SNOMED-CT } Congenital hypoplasia of finger (disorder) {78393008 , SNOMED-CT } Congenital hypoplasia of forepaw phalanx (disorder) {93257000 , SNOMED-CT } Congenital hypoplasia of fovea centralis (disorder) {429449002 , SNOMED-CT } Congenital hypoplasia of frontal bone (disorder) {93258005 , SNOMED-CT } Congenital hypoplasia of gallbladder (disorder) {93259002 , SNOMED-CT } Congenital hypoplasia of genital tubercle (disorder) {93260007 , SNOMED-CT } Congenital hypoplasia of heart (disorder) {93262004 , SNOMED-CT } Congenital hypoplasia of hindpaw phalanx (disorder) {93263009 , SNOMED-CT } Congenital hypoplasia of humerus (disorder) {93264003 , SNOMED-CT } Congenital hypoplasia of hyoid bone (disorder) {93265002 , SNOMED-CT } Congenital hypoplasia of ilium (disorder) {93266001 , SNOMED-CT } Congenital hypoplasia of interparietal bone (disorder) {93267005 , SNOMED-CT } Congenital hypoplasia of intestinal tract (disorder) {93268000 , SNOMED-CT } Congenital hypoplasia of ischium (disorder) {93269008 , SNOMED-CT } Congenital hypoplasia of kidney (disorder) {32659003 , SNOMED-CT } Congenital hypoplasia of lacrimal bone (disorder) {93270009 , SNOMED-CT } Congenital hypoplasia of metacarpal bone (disorder) {93272001 , SNOMED-CT } Congenital hypoplasia of metatarsal bone (disorder) {93273006 , SNOMED-CT } Congenital hypoplasia of nasal bone (disorder) {93274000 , SNOMED-CT } Congenital hypoplasia of ovary (disorder) {93279005 , SNOMED-CT } Congenital hypoplasia of palatine bone (disorder) {93281007 , SNOMED-CT } Congenital hypoplasia of pancreas (disorder) {68591005 , SNOMED-CT } Congenital hypoplasia of parietal bone (disorder) {93282000 , SNOMED-CT } Congenital hypoplasia of part of brain (disorder) {78693004 , SNOMED-CT } Congenital hypoplasia of paw (disorder) {93283005 , SNOMED-CT } Congenital hypoplasia of penis (disorder) {34911001 , SNOMED-CT } Congenital hypoplasia of premaxilla (disorder) {93284004 , SNOMED-CT } Congenital hypoplasia of presphenoid bone (disorder) {93285003 , SNOMED-CT } Congenital hypoplasia of pubis (disorder) {93286002 , SNOMED-CT } Congenital hypoplasia of radius (disorder) {93288001 , SNOMED-CT } Congenital hypoplasia of rib (disorder) {93291001 , SNOMED-CT } Congenital hypoplasia of spleen (disorder) {93292008 , SNOMED-CT } Congenital hypoplasia of squamosal bone (disorder) {93293003 , SNOMED-CT } Congenital hypoplasia of supraoccipital bone (disorder) {93294009 , SNOMED-CT } Congenital hypoplasia of tarsal bone (disorder) {93296006 , SNOMED-CT } Congenital hypoplasia of testis (disorder) {85437001 , SNOMED-CT } Congenital hypoplasia of thymus (disorder) {93297002 , SNOMED-CT } Congenital hypoplasia of tibia (disorder) {93298007 , SNOMED-CT } Congenital hypoplasia of tympanic anulus (disorder) {93299004 , SNOMED-CT } Congenital hypoplasia of ulna (disorder) {93300007 , SNOMED-CT } Congenital hypoplasia of urinary bladder (disorder) {93245009 , SNOMED-CT } Congenital hypoplasia of vas deferens (disorder) {93301006 , SNOMED-CT } Congenital hypoplasia of zygomatic bone (disorder) {93303009 , SNOMED-CT } Congenital hypotrichia (disorder) {56558005 , SNOMED-CT } Congenital insufficiency of heart valve NEC (disorder) {253262006 , SNOMED-CT } Congenital intestinal adhesions (disorder) {204748003 , SNOMED-CT } Congenital ischemic atrophy of central nervous system structure (disorder) {31076000 , SNOMED-CT } Congenital junctional epidermolysis bullosa-pyloric atresia syndrome (disorder) {53748002 , SNOMED-CT } Congenital keratoconus posticus circumscriptus (disorder) {75340008 , SNOMED-CT } Congenital kyphosis (disorder) {71311003 , SNOMED-CT } Congenital lacrimal fistula (disorder) {253220004 , SNOMED-CT } Congenital liver grooves (disorder) {20919000 , SNOMED-CT } Congenital lobulation of kidney (disorder) {13530005 , SNOMED-CT } Congenital lobulation of spleen (disorder) {42780004 , SNOMED-CT } Congenital lordosis/scoliosis (disorder) {287087003 , SNOMED-CT } Congenital lumbosacral stenosis (disorder) {7637004 , SNOMED-CT } Congenital malformation caused by valproic acid (disorder) {878878007 , SNOMED-CT } Congenital malformation of angle of anterior chamber of eye (disorder) {251729009 , SNOMED-CT } Congenital malformation of anterior abdominal wall (disorder) {253818009 , SNOMED-CT } Congenital malformation of anterior pituitary (disorder) {254255007 , SNOMED-CT } Congenital malformation of corpus callosum (disorder) {204042007 , SNOMED-CT } Congenital malformation of ear (disorder) {275259005 , SNOMED-CT } Congenital malformation of eye, ear and neck (disorder) {253204009 , SNOMED-CT } Congenital malformation of genital organs (disorder) {204821009 , SNOMED-CT } Congenital malformation of lymphatic system of cervicofacial region (disorder) {890372006 , SNOMED-CT } Congenital malformation of pancreas (disorder) {235977001 , SNOMED-CT } Congenital malformation of posterior pituitary (disorder) {254256008 , SNOMED-CT } Congenital malformation of salivary glands and ducts (disorder) {253755003 , SNOMED-CT } Congenital malformation of sphenoid wing (disorder) {431768007 , SNOMED-CT } Congenital malformation of sternum (disorder) {254041007 , SNOMED-CT } Congenital malformation of the eyebrow (disorder) {253206006 , SNOMED-CT } Congenital malformation of the meninges (disorder) {253199003 , SNOMED-CT } Congenital malformation of the respiratory system (disorder) {275260000 , SNOMED-CT } Congenital malformation of the urinary system (disorder) {253859003 , SNOMED-CT } Congenital malformation of tongue, mouth and pharynx (disorder) {253750008 , SNOMED-CT } Congenital malformation of upper alimentary tract (disorder) {275262008 , SNOMED-CT } Congenital malformation of vitreous humor (disorder) {253236002 , SNOMED-CT } Congenital malformation syndrome (disorder) {400038003 , SNOMED-CT } Congenital malformation syndromes due to known exogenous causes (disorder) {205787009 , SNOMED-CT } Congenital malformation syndromes with metabolic disturbances (disorder) {205826008 , SNOMED-CT } Congenital melanosis (disorder) {86042009 , SNOMED-CT } Congenital mesocolic hernia (disorder) {86595004 , SNOMED-CT } Congenital microgastria (disorder) {83714006 , SNOMED-CT } Congenital micrognathism (disorder) {32958008 , SNOMED-CT } Congenital misalignment of arch of caudal vertebra (disorder) {93370006 , SNOMED-CT } Congenital misalignment of arch of cervical vertebra (disorder) {93372003 , SNOMED-CT } Congenital misalignment of arch of lumbar vertebra (disorder) {93374002 , SNOMED-CT } Congenital misalignment of arch of sacral vertebra (disorder) {93379007 , SNOMED-CT } Congenital misalignment of arch of thoracic vertebra (disorder) {93382002 , SNOMED-CT } Congenital misalignment of centrum of caudal vertebra (disorder) {93371005 , SNOMED-CT } Congenital misalignment of centrum of cervical vertebra (disorder) {93373008 , SNOMED-CT } Congenital misalignment of centrum of lumbar vertebra (disorder) {93375001 , SNOMED-CT } Congenital misalignment of centrum of sacral vertebra (disorder) {93380005 , SNOMED-CT } Congenital misalignment of centrum of thoracic vertebra (disorder) {93383007 , SNOMED-CT } Congenital misalignment of palate rugae (disorder) {93376000 , SNOMED-CT } Congenital misalignment of pubis (disorder) {93377009 , SNOMED-CT } Congenital misalignment of rib (disorder) {93378004 , SNOMED-CT } Congenital misalignment of sternebra (disorder) {93381009 , SNOMED-CT } Congenital ocular coloboma (disorder) {93390002 , SNOMED-CT } Congenital omphalocele (disorder) {18735004 , SNOMED-CT } Congenital pigmented melanocytic nevus (disorder) {398696001 , SNOMED-CT } Congenital porencephaly (disorder) {38353004 , SNOMED-CT } Congenital postural lordosis (disorder) {24897005 , SNOMED-CT } Congenital postural scoliosis (disorder) {20944008 , SNOMED-CT } Congenital protrusion of tongue (disorder) {93391003 , SNOMED-CT } Congenital pseudoarthrosis of clavicle (disorder) {70794004 , SNOMED-CT } Congenital pseudoarthrosis of tibia (disorder) {55379003 , SNOMED-CT } Congenital pyloric membrane (disorder) {15419008 , SNOMED-CT } Congenital rectovaginal fistula (disorder) {111330004 , SNOMED-CT } Congenital rectovesical fistula (disorder) {64283009 , SNOMED-CT } Congenital red cell hypoplasia (disorder) {234372009 , SNOMED-CT } Congenital retinoschisis (disorder) {95493003 , SNOMED-CT } Congenital right ventricular diverticulum (disorder) {253525008 , SNOMED-CT } Congenital septal defect of heart (disorder) {59494005 , SNOMED-CT } Congenital septation of gallbladder (disorder) {22845004 , SNOMED-CT } Congenital short hard palate (disorder) {74622009 , SNOMED-CT } Congenital short tail (disorder) {93393000 , SNOMED-CT } Congenital skeletal dysplasia (disorder) {105986008 , SNOMED-CT } Congenital spade-like hand (disorder) {16585004 , SNOMED-CT } Congenital spinal meningocele (disorder) {65144005 , SNOMED-CT } Congenital stenosis of aortic arch (disorder) {93384001 , SNOMED-CT } Congenital stenosis of appendix (disorder) {253770002 , SNOMED-CT } Congenital stenosis of aqueduct of Sylvius (disorder) {50429003 , SNOMED-CT } Congenital stenosis of cardiac valve (disorder) {123657001 , SNOMED-CT } Congenital stenosis of cervical canal (disorder) {10283004 , SNOMED-CT } Congenital stenosis of colon (disorder) {253769003 , SNOMED-CT } Congenital stenosis of intestinal tract (disorder) {93386004 , SNOMED-CT } Congenital stenosis of mitral subvalvular apparatus (disorder) {449135007 , SNOMED-CT } Congenital stenosis of nasolacrimal duct (disorder) {271431003 , SNOMED-CT } Congenital stenosis of pulmonary veins (disorder) {11614003 , SNOMED-CT } Congenital stenosis of small intestine (disorder) {14430002 , SNOMED-CT } Congenital stenosis of stomach (disorder) {93387008 , SNOMED-CT } Congenital stenosis of vagina (disorder) {23544000 , SNOMED-CT } Congenital stenosis of vena cava (disorder) {88244008 , SNOMED-CT } Congenital stricture of anus (disorder) {204723001 , SNOMED-CT } Congenital stricture of bile duct (disorder) {1512006 , SNOMED-CT } Congenital stricture of external auditory canal (disorder) {43557002 , SNOMED-CT } Congenital stricture of osseous meatus of middle ear (disorder) {11144004 , SNOMED-CT } Congenital stricture of rectum (disorder) {39476006 , SNOMED-CT } Congenital stricture of ureter (disorder) {74919005 , SNOMED-CT } Congenital stricture of urethra (disorder) {13671009 , SNOMED-CT } Congenital stricture of urinary meatus (disorder) {48337000 , SNOMED-CT } Congenital stricture of vesicourethral orifice (disorder) {80797002 , SNOMED-CT } Congenital subaortic stenosis (disorder) {73660006 , SNOMED-CT } Congenital subpulmonary stenosis due to restrictive ventricular defect associated with functionally univentricular heart (disorder) {472801002 , SNOMED-CT } Congenital supravalvular mitral stenosis (disorder) {41514002 , SNOMED-CT } Congenital thoracostenosis (disorder) {93414008 , SNOMED-CT } Congenital thyroid hypoplasia (disorder) {237516005 , SNOMED-CT } Congenital urethrorectal fistula (disorder) {87093008 , SNOMED-CT } Congenital urethrovaginal fistula (disorder) {253837000 , SNOMED-CT } Congenital uterointestinal fistula (disorder) {204848005 , SNOMED-CT } Congenital valvular insufficiency (disorder) {1131009 , SNOMED-CT } Congenital vascular anomaly of eye (disorder) {2818004 , SNOMED-CT } Congenital vascular malformation (disorder) {400159008 , SNOMED-CT } Congenital web of esophagus (disorder) {89199004 , SNOMED-CT } Conjoined twins (disorder) {41337007 , SNOMED-CT } Cor biloculare (disorder) {81990004 , SNOMED-CT } Cor triloculare (disorder) {204397009 , SNOMED-CT } Cor triloculare biventriculare (disorder) {253276007 , SNOMED-CT } Cornea plana (disorder) {204145006 , SNOMED-CT } Craniorachischisis (disorder) {32219008 , SNOMED-CT } Cranioschisis (disorder) {48777005 , SNOMED-CT } Craniosynostosis syndrome (disorder) {57219006 , SNOMED-CT } Cutaneous asthenia in dogs AND/OR cats (disorder) {398242007 , SNOMED-CT } Cyst of paramesonephric duct (disorder) {721812005 , SNOMED-CT } Cyst of Wolffian duct (disorder) {204921008 , SNOMED-CT } Cystic malformation of posterior fossa (disorder) {35111000119109 , SNOMED-CT } Deep overbite (disorder) {60476005 , SNOMED-CT } Deformity due to amniotic band (disorder) {440214006 , SNOMED-CT } Dens evaginatus (disorder) {63691004 , SNOMED-CT } Developmental malformation of branchial arch (disorder) {402810002 , SNOMED-CT } Diaphyseal dysplasia (disorder) {34643004 , SNOMED-CT } Diastematomyelia (disorder) {49351009 , SNOMED-CT } Dimelia (disorder) {34488005 , SNOMED-CT } Discoid kidney (disorder) {37891007 , SNOMED-CT } Disorder: ectopic bone tissue, congenital (disorder) {26155004 , SNOMED-CT } Distal 16p11.2 microdeletion syndrome (disorder) {733521003 , SNOMED-CT } Distal 7q11.23 microdeletion syndrome (disorder) {770905005 , SNOMED-CT } Distal 7q11.23 microduplication syndrome (disorder) {773325004 , SNOMED-CT } Distal monosomy 12p (disorder) {770902008 , SNOMED-CT } Distal monosomy 7p syndrome (disorder) {782674007 , SNOMED-CT } Distal trisomy 20q syndrome (disorder) {764500002 , SNOMED-CT } Distal trisomy 7p syndrome (disorder) {763276000 , SNOMED-CT } Distal Xq28 microduplication syndrome (disorder) {773670004 , SNOMED-CT } Dominant dystrophic epidermolysis bullosa with absence of skin (disorder) {2689001 , SNOMED-CT } Double aortic valve (disorder) {77696009 , SNOMED-CT } Double auditory canal (disorder) {40320008 , SNOMED-CT } Double cardiac valve orifice (disorder) {36079008 , SNOMED-CT } Double kidney (disorder) {54967001 , SNOMED-CT } Double mitral valve (disorder) {78196008 , SNOMED-CT } Double monster (disorder) {43452005 , SNOMED-CT } Double outlet left atrium (disorder) {253426007 , SNOMED-CT } Doubly committed subarterial ventricular septal defect with muscular posterior inferior rim (disorder) {253570000 , SNOMED-CT } Duplication of teeth (disorder) {109458004 , SNOMED-CT } Dural arteriovenous malformation (disorder) {84873005 , SNOMED-CT } Dysmorphism (disorder) {276720006 , SNOMED-CT } Dysplasia of eye (disorder) {18821006 , SNOMED-CT } Ebstein's anomaly with atrial septal defect (disorder) {17394001 , SNOMED-CT } Ecchordosis physaliphora (disorder) {69664005 , SNOMED-CT } Ectodermal dysplasia (disorder) {8654005 , SNOMED-CT } Ectopia cordis (disorder) {78250005 , SNOMED-CT } Ectopic adrenal gland (disorder) {49494003 , SNOMED-CT } Ectopic breast tissue (disorder) {1896004 , SNOMED-CT } Ectopic cilia of eyelid (disorder) {95504004 , SNOMED-CT } Ectopic gallbladder (disorder) {87541004 , SNOMED-CT } Ectopic gastric tissue (disorder) {70450006 , SNOMED-CT } Ectopic glial tissue (disorder) {43427008 , SNOMED-CT } Ectopic gray matter in centrum ovale (disorder) {54794009 , SNOMED-CT } Ectopic hyperparathyroidism (disorder) {29326002 , SNOMED-CT } Ectopic intestinal mucosa (disorder) {61108006 , SNOMED-CT } Ectopic kidney (disorder) {16507009 , SNOMED-CT } Ectopic neuronal tissue (disorder) {266673001 , SNOMED-CT } Ectopic oral gastrointestinal cyst (disorder) {109554004 , SNOMED-CT } Ectopic ovary (disorder) {62524003 , SNOMED-CT } Ectopic pancreas (disorder) {19387007 , SNOMED-CT } Ectopic pituitary tissue (disorder) {6537000 , SNOMED-CT } Ectopic pupil (disorder) {193523008 , SNOMED-CT } Ectopic spleen (disorder) {65146007 , SNOMED-CT } Ectopic testis (disorder) {50911000 , SNOMED-CT } Ectopic thymic tissue (disorder) {17422006 , SNOMED-CT } Ectopic tooth (disorder) {43162008 , SNOMED-CT } Ectopic ureter (disorder) {44796002 , SNOMED-CT } Ectrodactyly (disorder) {81208006 , SNOMED-CT } Eisenmenger's defect (disorder) {83130006 , SNOMED-CT } Embryological remnant (disorder) {276752006 , SNOMED-CT } Embryonic cyst of Gartner's duct (disorder) {82520000 , SNOMED-CT } Encephalocele (disorder) {55999004 , SNOMED-CT } Endocardial cushion defect (disorder) {15459006 , SNOMED-CT } Fallot's trilogy (disorder) {204351007 , SNOMED-CT } Fetus with central nervous system malformation (disorder) {267252001 , SNOMED-CT } Fistula of branchial cleft (disorder) {204268008 , SNOMED-CT } Fistula of congenital auricle (disorder) {204276005 , SNOMED-CT } Flat palate (disorder) {253751007 , SNOMED-CT } Foramen of Luschka atresia (disorder) {204062004 , SNOMED-CT } Foramen of Magendie atresia (disorder) {204061006 , SNOMED-CT } Fordyce spots of buccal mucosa (disorder) {403369005 , SNOMED-CT } Fordyce's disease (disorder) {50584008 , SNOMED-CT } FRAXE intellectual disability syndrome (disorder) {716709002 , SNOMED-CT } FRAXF syndrome (disorder) {716708005 , SNOMED-CT } Fundus coloboma (disorder) {39302008 , SNOMED-CT } Fused commissures of mitral valve (disorder) {91634006 , SNOMED-CT } Fused mitral papillary muscles (disorder) {253412003 , SNOMED-CT } Fused tricuspid papillary muscle (disorder) {253393005 , SNOMED-CT } Fusion of kidneys (disorder) {204984002 , SNOMED-CT } Fusion of teeth (disorder) {1744008 , SNOMED-CT } Gastric atresia (disorder) {28828001 , SNOMED-CT } Gastroschisis (disorder) {72951007 , SNOMED-CT } Geographic retinal dysplasia (disorder) {95496006 , SNOMED-CT } Gingival odontogenic cyst (disorder) {58271001 , SNOMED-CT } Gynandromorphism syndrome (disorder) {123644009 , SNOMED-CT } Hemianencephaly (disorder) {85641006 , SNOMED-CT } Hemicardia (disorder) {204399007 , SNOMED-CT } Hemimyelia (disorder) {73331006 , SNOMED-CT } Hereditary elliptocytosis (disorder) {191169008 , SNOMED-CT } Hereditary mucoepithelial dysplasia (disorder) {403442005 , SNOMED-CT } Hologastroschisis (disorder) {93556005 , SNOMED-CT } Horizontal overbite (disorder) {70305005 , SNOMED-CT } Hutchinson's teeth (disorder) {86443005 , SNOMED-CT } Hydrencephalomeningocele (disorder) {410060009 , SNOMED-CT } Hydrocephalus associated with congenital aqueduct stenosis (disorder) {302882002 , SNOMED-CT } Hydromeningocele (disorder) {25129008 , SNOMED-CT } Hydromicrocephaly (disorder) {78071008 , SNOMED-CT } Hydromyelia (disorder) {11197005 , SNOMED-CT } Hyperextension deformity of knee (disorder) {65621006 , SNOMED-CT } Hypopigmentation-immunodeficiency disease (disorder) {37548006 , SNOMED-CT } Hypoplasia of eye (disorder) {86527000 , SNOMED-CT } Hypospadias (disorder) {416010008 , SNOMED-CT } Incomplete congenital absence of thigh AND leg (disorder) {16904009 , SNOMED-CT } Incomplete development of membranous labyrinth (disorder) {70583001 , SNOMED-CT } Infection causing congenital anomaly (disorder) {721282005 , SNOMED-CT } Infundibular pulmonic stenosis (disorder) {3192005 , SNOMED-CT } Intercostal rib (disorder) {93615001 , SNOMED-CT } Isodicentric chromosome 15 syndrome (disorder) {723332005 , SNOMED-CT } Jackson's membrane (disorder) {28016005 , SNOMED-CT } Jeune thoracic dystrophy (disorder) {75049004 , SNOMED-CT } Kasabach-Merritt syndrome (disorder) {86635005 , SNOMED-CT } Keratoconus (disorder) {65636009 , SNOMED-CT } Kohlschutter's syndrome (disorder) {109478007 , SNOMED-CT } Leptocephaly (disorder) {93131008 , SNOMED-CT } Lip pits (disorder) {235141009 , SNOMED-CT } Lymphatic malformation (disorder) {234095009 , SNOMED-CT } Macromelia (disorder) {93180003 , SNOMED-CT } Macropalpebral fissure (disorder) {95503005 , SNOMED-CT } Malformation of tooth (disorder) {422775003 , SNOMED-CT } Manus cava (disorder) {45615004 , SNOMED-CT } Membranous ventricular septum defect (disorder) {94150003 , SNOMED-CT } Meningomyelocele (disorder) {7096005 , SNOMED-CT } Microcystic renal disease (disorder) {57088004 , SNOMED-CT } Microdeletion of chromosome 15q13.3 (disorder) {699254009 , SNOMED-CT } Microglossia (disorder) {32614006 , SNOMED-CT } Microtia (disorder) {35045004 , SNOMED-CT } Monster (disorder) {54900001 , SNOMED-CT } Mosaic trisomy 10 syndrome (disorder) {764461004 , SNOMED-CT } Mullerian aplasia (disorder) {253828000 , SNOMED-CT } Multiple congenital malformations (disorder) {116022009 , SNOMED-CT } Multiple gastrointestinal atresias (disorder) {95472001 , SNOMED-CT } Muscular ventricular septum defect (disorder) {94706008 , SNOMED-CT } Myelatelia (disorder) {29956001 , SNOMED-CT } Myelocele (disorder) {82058009 , SNOMED-CT } Myeloschisis (disorder) {360530005 , SNOMED-CT } Neck webbing (disorder) {11731003 , SNOMED-CT } Neuronal choristoma (disorder) {230794008 , SNOMED-CT } Nicolaides-Baraitser syndrome (disorder) {401046009 , SNOMED-CT } Oculootodental syndrome (disorder) {770944002 , SNOMED-CT } Pancreas divisum (disorder) {54554009 , SNOMED-CT } Parachute malformation of mitral valve (disorder) {204362007 , SNOMED-CT } Partial aphalangia of lower limb (disorder) {59070002 , SNOMED-CT } Partial congenital absence of limb (disorder) {60220000 , SNOMED-CT } Paternal 14q32.2 microdeletion (disorder) {1003449005 , SNOMED-CT } Peg-shaped teeth (disorder) {29553002 , SNOMED-CT } Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome (disorder) {1172899000 , SNOMED-CT } Perodactylia (disorder) {253970009 , SNOMED-CT } Persistent convolutions of aortic arch (disorder) {87280006 , SNOMED-CT } Phocomelia (disorder) {22841008 , SNOMED-CT } Pilonidal cyst with abscess (disorder) {85224001 , SNOMED-CT } Pilonidal cyst without abscess (disorder) {76545008 , SNOMED-CT } Placenta accreta (disorder) {70129008 , SNOMED-CT } Platybasia (disorder) {86587003 , SNOMED-CT } Platyspondylia (disorder) {7603007 , SNOMED-CT } Pleonotia (disorder) {75832005 , SNOMED-CT } Pleuropericardial cyst (disorder) {253733006 , SNOMED-CT } Polycystic kidney disease, infantile type (disorder) {28770003 , SNOMED-CT } Polydactyly (disorder) {367506006 , SNOMED-CT } Polymelia (disorder) {89243009 , SNOMED-CT } Polyorchism (disorder) {17471001 , SNOMED-CT } Polyotia (disorder) {35547002 , SNOMED-CT } Preauricular cyst (disorder) {18820007 , SNOMED-CT } Preauricular sinus (disorder) {204271000 , SNOMED-CT } Premature closure of foramen ovale (disorder) {19249002 , SNOMED-CT } Protrusion of tooth (finding) {109507003 , SNOMED-CT } Proximal 16p11.2 microdeletion syndrome (disorder) {718227006 , SNOMED-CT } Proximal 16p11.2 microduplication syndrome (disorder) {765142003 , SNOMED-CT } Rathke's pouch cyst (disorder) {52859009 , SNOMED-CT } Regional odontodysplasia (disorder) {66063001 , SNOMED-CT } Renal agenesis (disorder) {204942005 , SNOMED-CT } Renal dysplasia (disorder) {204949001 , SNOMED-CT } Retinal hemangioblastomatosis (disorder) {2167004 , SNOMED-CT } Retinitis pigmentosa-deafness syndrome (disorder) {57838006 , SNOMED-CT } Right ventricular outflow tract atresia (disorder) {253533009 , SNOMED-CT } Roger's disease (disorder) {80387009 , SNOMED-CT } Rudimentary patella (disorder) {79991006 , SNOMED-CT } Sacral agenesis (disorder) {205425003 , SNOMED-CT } Scaphycephaly (disorder) {4191007 , SNOMED-CT } Septate vagina (disorder) {47054003 , SNOMED-CT } Shell teeth (disorder) {67504007 , SNOMED-CT } Short stature, facial and skeletal anomalies, intellectual disability, macrodontia syndrome (disorder) {711156009 , SNOMED-CT } Short supernumerary rib (disorder) {95265004 , SNOMED-CT } Single congenital anomaly (disorder) {698601005 , SNOMED-CT } Sinus pericranii (disorder) {50751005 , SNOMED-CT } Sirenoform monster (disorder) {67254002 , SNOMED-CT } Situs ambiguus (disorder) {14821001 , SNOMED-CT } Situs inversus viscerum (disorder) {43876007 , SNOMED-CT } Spina bifida (disorder) {67531005 , SNOMED-CT } Spinal hydromeningocele (disorder) {203967002 , SNOMED-CT } Spinal meningocele (disorder) {203978005 , SNOMED-CT } Splenogonadal fusion (disorder) {62042001 , SNOMED-CT } Spondyloschisis (disorder) {30028006 , SNOMED-CT } Stenosis of infundibulum of right ventricle (disorder) {204370002 , SNOMED-CT } Sternum bifidum (disorder) {54008006 , SNOMED-CT } Structural developmental anomalies of neurenteric canal (disorder) {249491000119100 , SNOMED-CT } Sturge-Weber syndrome (disorder) {19886006 , SNOMED-CT } Supernumerary azygos vein (disorder) {95286004 , SNOMED-CT } Supernumerary cusps of mitral valve (disorder) {21776004 , SNOMED-CT } Supernumerary cusps of the mitral valve (disorder) {204363002 , SNOMED-CT } Supernumerary deciduous tooth (disorder) {109448003 , SNOMED-CT } Supernumerary eye muscle (disorder) {85697009 , SNOMED-CT } Supernumerary forepaw phalanx (disorder) {95294006 , SNOMED-CT } Supernumerary fused sternebra (disorder) {95295007 , SNOMED-CT } Supernumerary gallbladder (disorder) {91844006 , SNOMED-CT } Supernumerary hindpaw phalanx (disorder) {95296008 , SNOMED-CT } Supernumerary mesiodens tooth (disorder) {17802000 , SNOMED-CT } Supernumerary metacarpal bone (disorder) {91846008 , SNOMED-CT } Supernumerary metatarsal bone (disorder) {95299001 , SNOMED-CT } Supernumerary pulmonary valve cusps (disorder) {204352000 , SNOMED-CT } Supernumerary roots (disorder) {12270007 , SNOMED-CT } Supernumerary tarsal bone (disorder) {95301008 , SNOMED-CT } Supernumerary tooth (disorder) {367534004 , SNOMED-CT } Supernumerary vertebra (disorder) {87294007 , SNOMED-CT } Synchilia (disorder) {54764003 , SNOMED-CT } Synechia vulvae (disorder) {13262009 , SNOMED-CT } Talipomanus (disorder) {16603000 , SNOMED-CT } Tetralogy of Fallot (disorder) {86299006 , SNOMED-CT } Thoracoceloschisis (disorder) {93413002 , SNOMED-CT } Totally absent pericardium (disorder) {253732001 , SNOMED-CT } Trifid pelvis of kidney (disorder) {59758007 , SNOMED-CT } Trifid tongue (disorder) {12721007 , SNOMED-CT } Trisomy 13 - mitotic nondisjunction mosaicism (disorder) {205620000 , SNOMED-CT } Trisomy 13, meiotic nondisjunction (disorder) {205619006 , SNOMED-CT } Tuberculum paramolare (disorder) {78305006 , SNOMED-CT } Turner's tooth (disorder) {10078003 , SNOMED-CT } Uhl's disease (disorder) {2829000 , SNOMED-CT } Unilateral agenesis of kidney (situation) {55726006 , SNOMED-CT } Upper esophageal web (disorder) {11266002 , SNOMED-CT } Ureterocele (disorder) {12818004 , SNOMED-CT } Vascular anomaly of umbilical cord (disorder) {31481000 , SNOMED-CT } Venous malformation (disorder) {234124003 , SNOMED-CT } Ventricular septal defect in Fallot's tetralogy (disorder) {253515003 , SNOMED-CT } Ventricular septal defect with malaligned outlet septum (disorder) {448062009 , SNOMED-CT } Weill-Marchesani syndrome (disorder) {2884008 , SNOMED-CT }