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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

In OMIM:
OMIM:605389 - HYPOTRICHOSIS 1; HYPT1

In Mondo Disease Ontology:
MONDO:0011549 - hypotrichosis 1

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : tgif1, apcdd1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): hypotrichosis (is_a)