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DOID:0060655 - autosomal recessive congenital ichthyosis
Disease Ontology Definition:A skin disease that is characterized by autosomal recessive inheritance and abnormal skin scaling over the whole body due to a defect in keratinization.
Synonyms: ARCI,
Echinobase Genes : tgm1
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
skin disease (is_a)