Skip to main content
Diseases

Cutis Laxa

cutis laxa

Entity Type
Diseases
Relation Groups
4
Relation Preview
32

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

Identifiers

DO ID
No data
MeSH ID
D003483
OMIM ID
MTHU006920|MTHU035760|MTHU007951|MTHU011913
UMLS ID
C0010495
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:A congenital or acquired disorder affecting the elastic fibers of the skin. It is characterized by loss of elasticity resulting in loosening and folding of the skin.|MSH2017_2016_08_12:A group of connective tissue diseases in which skin hangs in loose pendulous folds. It is believed to be associated with decreased elastic tissue formation as well as an abnormality in elastin formation. Cutis laxa is usually a genetic disease, but acquired cases have been reported. (From Dorland, 27th ed)|HPO2016_07_04:Wrinkled, redundant, inelastic and sagging skin. [HPO:probinson]|CSP2006:group of connective tissue diseases in which skin hangs in loose pendulous folds; believed to be associated with decreased elastic tissue formation as well as an abnormality in elastin formation; usually a genetic disease, but acquired cases have been reported.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
03
EZH2
enhancer of zeste 2 polycomb repressive complex 2 subunit
enhancer of zeste 2 polycomb repressive complex 2 subunit