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.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
This disease has been annotated by GARD as a rare disease.
Description from Mondo Disease Ontology.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
COHD:4242416
DOID:3144
GARD:0006227
MESH:D003483
NCIT:C84663
Orphanet:209
SCTID:58588007
UMLS:C0010495
MONDO:0016175
High level summary of knowledge for a disease, including descriptions and datasource references.