Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0110698 - hypotrichosis 1

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

Synonyms: hereditary generalized hypotrichosis simplex, Hhs, HHS, Hts, HTS, Hypt1, HYPT1

Xenbase Genes : tgif1, apcdd1

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

MIM:
MIM:605389 - HYPOTRICHOSIS 1; HYPT1

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)