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Summary Literature (0)
DOID:0110705 - hypotrichosis 8

Disease Ontology Definition:A hypotrichosis has_material_basis_in a autosomal recessive mutation of the LPAR6 gene on chromosome 13q14.2.

Synonyms: hypotrichosis, localized, autosomal recessive 3, Hypt8, HYPT8, Lah3, LAH3

Xenbase Genes : lpar6

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010206 - hypotrichosis 8


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), hypotrichosis (is_a)