OBO ID: DOID:0080353 |
Term Name: | X-linked recessive hypophosphatemic rickets | Search Ontology: | |
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Definition: | A rickets that has_material_basis_in mutation in the CLCN5 gene on chromosome Xp11.22. https://ghr.nlm.nih.gov/condition/hereditary-hypophosphatemic-rickets | ||
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Ontology: | Human Disease ( DOID:0080353 ) |
OTHER X-linked recessive hypophosphatemic rickets PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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