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| Term | hypotrichosis 8 | ID (Ontology) | DOID:0110705 (Human Disease) |
| Definition | A hypotrichosis has_material_basis_in a autosomal recessive mutation of the LPAR6 gene on chromosome 13q14.2. | ||
| Also Known As | "hypotrichosis, localized, autosomal recessive 3" ; "HYPT8" ; "LAH3" | ||
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autosomal genetic disease |__autosomal recessive disease__ hair disease | |__hypotrichosis________________| hypotrichosis 8 |
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| Is a |
autosomal recessive disease hypotrichosis |
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| MIM:278150 | |||