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DOID:4535 - hypotrichosis
Disease Ontology Definition:A hair disease that is characterized by sparse hair on the scalp resulting from abnormal hair follicle development and has_material_basis_in mutations in proteins involved in hair growth, division or proliferation of cells within hair follicles.
Synonyms:
Xenbase Genes
:
cdh3,
tgif1,
rpl21,
apcdd1,
liph,
snrpe,
lpar6
| MONDO:0003037 - hypotrichosis |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hair disease (is_a)