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Summary Literature (0)
DOID:0110708 - hypotrichosis 11

Disease Ontology Definition:A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the SNRPE gene on chromosome 1q32.1.

Synonyms: Hypt11, HYPT11

Xenbase Genes : snrpe

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014027 - hypotrichosis 11


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)