|
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
OMIM:605389 - HYPOTRICHOSIS 1; HYPT1 |
MONDO:0011549 - hypotrichosis 1 |
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes

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