Search Ontology:
Human Disease
hypotrichosis 7
- Term ID
- DOID:0110704
- Synonyms
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- hypotrichosis, localized, autosomal recessive 2
- HYPT7
- LAH2
- total hyptrichosis, Mari type
- Definition
- A hypotrichosis that has_material_basis_in a autosomal recessive mutation of the LIPH gene on chromosome 3q27.2. https://www.ncbi.nlm.nih.gov/pubmed/20393562
- References
- Ontology
- Human Disease ( DOID:0110704 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models