Summary Literature (0)

DOID:3144 - cutis laxa

Disease Ontology Definition:A skin disease characterized by loose, hanging, wrinkled skin lacking in elasticity.

Synonyms: Cutis laxa, loose skin,

Echinobase Genes :


OMIM:

MIM:123700 - cutis laxa, autosomal dominant 1; adcl1

MIM:219100 - cutis laxa, autosomal recessive, type ia; arcl1a

MIM:219150 - cutis laxa, autosomal recessive, type iiia; arcl3a

MIM:219200 - cutis laxa, autosomal recessive, type iia; arcl2a

MIM:612940 - cutis laxa, autosomal recessive, type iib; arcl2b

MIM:613177 - cutis laxa, autosomal recessive, type ic; arcl1c

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee