autosomal dominant cutis laxa

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Summary

Literature (0)

DOID:0070142 - autosomal dominant cutis laxa

Disease Ontology Definition:A cutis laxa characterized by autosomal dominant inheritance of skin that is loose, hanging, wrinkled and lacking in elasticity.

Synonyms: ADCL

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: atp6v1a, atp6v0a2, fbln5, atp6v1e1, aldh18a1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0019571 - autosomal dominant cutis laxa

MONDO:0019571 - autosomal dominant cutis laxa

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

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

Parent(s): autosomal dominant disease (is_a), cutis laxa (is_a)