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DOID:0070141 - autosomal recessive cutis laxa type II classic type
Disease Ontology Definition:A cutis laxa characterized by generalized skin wrinkling, sparse subcutaneous fat, dysmorphic progeroid facial features and severe hypotonia.
Synonyms: ARCL2, Debre type, ARCL2, classic type,
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
cutis laxa (is_a)