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Diseases

Autosomal Dominant Cutis Laxa

autosomal dominant cutis laxa

Entity Type
Diseases
Relation Groups
3
Relation Preview
19

Basic Information

Grouped by core information, identifiers, and descriptions.

Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name
Autosomal Dominant Cutis Laxa
Standard Disease Name
autosomal dominant cutis laxa
MeSH Tree
No data
ICD-10
Q82.8

Identifiers

DO ID
No data
MeSH ID
C562627
OMIM ID
123700|616603|614434
UMLS ID
C0268350
HPO ID
No data

Description and Extensions

Description
Autosomal dominant cutis laxa (ADCL) is a connective tissue disorder characterized by wrinkled, redundant and sagging inelastic skin associated in some cases with internal organ involvement.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease3 Targets
01
ALDH18A1
aldehyde dehydrogenase 18 family member A1
aldehyde dehydrogenase 18 family member A1