autosomal recessive congenital ichthyosis 3

Summary

DOID:0060711 - autosomal recessive congenital ichthyosis 3

Disease Ontology Definition:An autosomal recessive congenital ichthyosis characterized by mild ichthyosis, fine scales on the scalp, face, trunk and limbs, dark brown adherent scales on the neck, elbow and knees, and hypohydrosis that has_material_basis_in homozygous or compound heterozygous mutation in the ALOXE3 gene on chromosome 17p13.

Synonyms: ARCI3, lamellar ichthyosis 5,

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

: aloxe3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011680 - autosomal recessive congenital ichthyosis 3

MONDO:0011680 - autosomal recessive congenital ichthyosis 3

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

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

Parent(s): autosomal recessive congenital ichthyosis (is_a)