Search Ontology:
Human Disease
hypotrichosis 8
- Term ID
- DOID:0110705
- Synonyms
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- hypotrichosis, localized, autosomal recessive 3
- HYPT8
- LAH3
- Definition
- A hypotrichosis has_material_basis_in a autosomal recessive mutation of the LPAR6 gene on chromosome 13q14.2. https://www.ncbi.nlm.nih.gov/pubmed/18297072
- References
- Ontology
- Human Disease ( DOID:0110705 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models