OBO ID: DOID:0110710 |
Term Name: | hypotrichosis 13 | Search Ontology: | |
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Synonyms: |
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Definition: | A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the KRT71 gene on chromosome 12q13.13. https://www.ncbi.nlm.nih.gov/pubmed/22592156 | ||
References: | |||
Ontology: | Human Disease ( DOID:0110710 ) |
OTHER hypotrichosis 13 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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KRT71 | ?Hypotrichosis 13 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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