OBO ID: DOID:0110707 |
Term Name: | hypotrichosis 10 | Search Ontology: | |
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Definition: | A hypotrichosis that has_material_basis_in an autosomal recessive mutation on chromosome 7p22.3-p21.3. https://www.ncbi.nlm.nih.gov/pubmed/20544222 | ||
References: | |||
Ontology: | Human Disease ( DOID:0110707 ) |
OTHER hypotrichosis 10 PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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