Code System Concept

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Code System Concept

Code System Concept Code	77016009
Code System Concept Name	Amyoplasia congenita disruptive sequence (disorder)
Code System Preferred Concept Name	Amyoplasia congenita disruptive sequence (disorder)
Concept Status	Published
Concept Status Date	09/01/2024
Code System Name	SNOMED-CT

Concept Relationships
Concept Details

Concept Details

Code System Code	PH_SNOMED-CT
Code System OID	2.16.840.1.113883.6.96
HL7 Table 0396 Code	SCT
Superseded By Concept
SDO Concept Status	Inactive
SDO Concept Status Date	01/31/2002
SDO Date Created	01/31/2002
SDO Date Revised	02/28/2023
Description
Sequence

Extended Properties

No extended properties.

Concept Alternate Designations

SDO Designation ID	Concept Designation Description	Status	Designation Type	PHIN Preferred Term Flag	Code Flag
127855010	Amyoplasia congenita disruptive sequence	Active	Synonym	false	false
127856011	Myodystrophia foetalis deformans	Active	Synonym	false	false
127857019	Classic arthrogryposis	Active	Synonym	false	false
127858012	Arthrogryposis multiplex congenita	Active	Synonym	false	false
127859016	Myodystrophia fetalis deformans	Active	Synonym	false	false
127860014	Multiple congenital articular rigidities	Active	Synonym	false	false
127861013	Congenital arthromyodysplasia	Active	Synonym	false	false
127862018	Myophagism congenita	Active	Synonym	false	false
127863011	Amyoplasia congenita	Active	Synonym	false	false
127864017	Congenital multiple arthrogryposis	Active	Synonym	false	false
503436016	AMC - Arthrogryposis multiplex congenita	Active	Synonym	false	false

Associated Value Sets

Value Set Name	Version(s)
Disease	10 , 9 , 8 , 7 , 6 , 5 , 4 , 3 , 2 , 1
Problem Value Set	3 , 2 , 1

Parent Concepts

Parent Concepts

Parent/Child (Relationship Type)

Arthrogryposis (disorder) {111246005 , SNOMED-CT } Congenital anomaly of joint (disorder) {95463009 , SNOMED-CT } Congenital anomaly of skeletal muscle (disorder) {89886004 , SNOMED-CT } Disorder of skeletal muscle (disorder) {75047002 , SNOMED-CT } Multiple malformation syndrome with unusual brain and/or neuromuscular findings (disorder) {64162006 , SNOMED-CT } Muscle contracture (disorder) {55033002 , SNOMED-CT }

Other Relationships

No other relationships present.

Child Concepts

Amyoplasia congenita disruptive sequence (disorder) {77016009 , SNOMED-CT }

Parent/Child (Relationship Type)

Adducted thumbs and arthrogryposis syndrome Christian type (disorder) {720463009 , SNOMED-CT } Arthrogryposis hyperkeratosis syndrome lethal form (disorder) {726620005 , SNOMED-CT } Arthrogryposis multiplex congenita and whistling face syndrome (disorder) {720514008 , SNOMED-CT } Autosomal recessive myogenic arthrogryposis multiplex congenita (disorder) {764812008 , SNOMED-CT } Congenital lethal myopathy Compton North type (disorder) {773306002 , SNOMED-CT } Hypomyelination neuropathy arthrogryposis syndrome (disorder) {766931003 , SNOMED-CT } Intellectual disability, developmental delay, contracture syndrome (disorder) {722456001 , SNOMED-CT } Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder) {715565004 , SNOMED-CT } Van den Ende-Gupta syndrome (disorder) {719845008 , SNOMED-CT } X-linked distal arthrogryposis multiplex congenita (disorder) {719836007 , SNOMED-CT }

Page last reviewed:June 20, 2024
Page last updated:June 20, 2024
Content source:
- Centers for Disease Control and Prevention,