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cutis laxa

Disease Summary
Associated Targets (16)
Tbio

14

Tchem

2


Explore Associated Targets
Mondo Description Cutis laxa (CL) is an inherited or acquired connective tissue disorder characterized by wrinkled, redundant and sagging inelastic skin associated with skeletal and developmental anomalies and, in some cases, with severe systemic involvement. Several different forms of inherited CL have been described, differentiated on the basis of the mode of inheritance and differences in the extent of internal organ involvement, associated anomalies and disease severity.
Disease Ontology Description A skin disease characterized by loose, hanging, wrinkled skin lacking in elasticity.
Mondo Term and Equivalent IDs
MONDO:0016175:  cutis laxa
COHD:4242416: 
GARD:0006227: 
MESH:D003483: 
NCIT:C84663: 
Orphanet:209: 
SCTID:58588007: 
UMLS:C0010495: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)