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Summary Literature (0)
DOID:0110698 - hypotrichosis 1


Disease Ontology Definition:A hypotrichosis that has_material_basis_in a autosomal dominant mutation of APCDD1 on chromosome 18p11.22.

Synonyms: Hhs, Hts, Hypt1, hereditary generalized hypotrichosis simplex

Xenbase Genes : tgif1, apcdd1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011549 - hypotrichosis 1

OMIM:
OMIM:605389 - HYPOTRICHOSIS 1; HYPT1

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hypotrichosis (is_a)