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Summary Literature (0)
DOID:0110702 - hypotrichosis 5

Disease Ontology Definition:A hypotrichosis that has_material_basis_in a mutation on chromosome 1p21.1-q21.3.

Synonyms: Hypt5, Marie Unna Hereditary Hypotrichosis 2, Muhh2,

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013017 - hypotrichosis 5


Other Model Organisms: AGR, 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)