Search Ontology:
Human Disease
hypotrichosis 12
- Term ID
- DOID:0110709
- Synonyms
-
- Hypt12
- Definition
- A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the RPL21 gene on chromosome 13q12.2. https://www.ncbi.nlm.nih.gov/pubmed/21412954
- References
- Ontology
- Human Disease ( DOID:0110709 )
- is a type of
-
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