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Summary Literature (0)
DOID:0110709 - hypotrichosis 12

Disease Ontology Definition:A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the RPL21 gene on chromosome 13q12.2.

Synonyms: Hypt12, HYPT12

Xenbase Genes : rpl21

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014384 - hypotrichosis 12

MIM:
MIM:615885 - HYPOTRICHOSIS 12; HYPT12

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), hypotrichosis (is_a)