OBO ID: DOID:0110709 |
Term Name: | hypotrichosis 12 | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0110709 ) |
OTHER hypotrichosis 12 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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