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DOID:0110705 - hypotrichosis 8
Disease Ontology Definition:A hypotrichosis has_material_basis_in a autosomal recessive mutation of LPAR6 on chromosome 13q14.2.
Synonyms: Hypt8, Lah3, hypotrichosis, localized, autosomal recessive 3,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MIM:278150 - hypotrichosis 8; hypt8 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hypotrichosis (is_a)