Code System Concept

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Code System Concept

Code System Concept Code	58588007
Code System Concept Name	Cutis laxa (disorder)
Code System Preferred Concept Name	Cutis laxa (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Superseded By Concept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	Active
SDO Concept Status Date	01/31/2002
SDO Date Created	01/31/2002
SDO Date Revised	01/31/2002
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
1783830011	Systematised elastorrhexis	Active	Synonym	false	false
1784217012	Systematized elastorrhexis	Active	Synonym	false	false
1788072014	Systemic elastorrhexis	Active	Synonym	false	false
2478767011	Dermatochalasis	Active	Synonym	false	false
498198019	Generalised dermatochalasis	Active	Synonym	false	false
498199010	Generalised elastorrhexis	Active	Synonym	false	false
498200013	Generalised elastolysis	Active	Synonym	false	false
498201012	Generalized dermatochalasis	Active	Synonym	false	false
498202017	Generalized elastolysis	Active	Synonym	false	false
498203010	Generalized elastorrhexis	Active	Synonym	false	false
97359016	Cutis laxa	Active	Synonym	false	false
97361013	Dermatochalasia	Active	Synonym	false	false
97362018	Primary elastolysis	Active	Synonym	false	false
97363011	Chalazodermia	Active	Synonym	false	false
97365016	Dermatomegaly	Active	Synonym	false	false
97366015	Dermatolysis	Active	Synonym	false	false

Associated Value Sets

Value Set Name	Version(s)
Clinical Finding (NNDSS)	2 , 1
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)

Collagen and elastic tissue disorders affecting skin (disorder) {238846003 , SNOMED-CT } Congenital anomaly of integument (disorder) {38164009 , SNOMED-CT } Disorder of skin (disorder) {95320005 , SNOMED-CT } Hereditary disorder of the integument (disorder) {363185004 , SNOMED-CT } Metabolic disease of collagen (disorder) {73873008 , SNOMED-CT }

Other Relationships

No other relationships present.

Child Concepts

Cutis laxa (disorder) {58588007 , SNOMED-CT }

Parent/Child (Relationship Type)

Cantu's syndrome (disorder) {239087008 , SNOMED-CT } Congenital/hereditary cutis laxa (disorder) {402783001 , SNOMED-CT } Craniofaciofrontodigital syndrome (disorder) {763320005 , SNOMED-CT } Cutis laxa of bilateral lower eyelid (disorder) {10743351000119102 , SNOMED-CT } Cutis laxa of bilateral upper eyelid (disorder) {10743311000119103 , SNOMED-CT } Cutis laxa of lower eyelid (disorder) {442009005 , SNOMED-CT } Cutis laxa of upper eyelid (disorder) {441963008 , SNOMED-CT } Cutis laxa secondary to inherited disorder of connective tissue (disorder) {403814004 , SNOMED-CT } Cutis laxa senilis (disorder) {5280003 , SNOMED-CT } Cutis laxa with osteodystrophy (disorder) {73856006 , SNOMED-CT } Cutis laxa, acquired type (disorder) {19726003 , SNOMED-CT } de Barsey syndrome (disorder) {59252009 , SNOMED-CT } Drug-induced cutis laxa (disorder) {403672006 , SNOMED-CT } Hemolytic anemia with emphysema AND cutis laxa (disorder) {60805002 , SNOMED-CT } Idiopathic mid-dermal elastolysis (disorder) {238821003 , SNOMED-CT } Inherited cutis laxa (disorder) {254220005 , SNOMED-CT } Localized abdominal wall skin atrophy (disorder) {238827004 , SNOMED-CT } Noninflammatory dermal elastolysis (disorder) {238822005 , SNOMED-CT }

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