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Summary Literature (0)
DOID:0110704 - hypotrichosis 7

Disease Ontology Definition:A hypotrichosis that has_material_basis_in a autosomal recessive mutation of the LIPH gene on chromosome 3q27.2.

Synonyms: hypotrichosis, localized, autosomal recessive 2, Hypt7, HYPT7, Lah2, LAH2, total hyptrichosis, Mari type, total Mari type hypotrichosis,

Xenbase Genes : liph

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011452 - hypotrichosis 7

MIM:
MIM:604379 - HYPOTRICHOSIS 7; HYPT7

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)