Search Ontology:
Human Disease
X-linked recessive hypophosphatemic rickets
- Term ID
- DOID:0080353
- Synonyms
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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
- References
- Ontology
- Human Disease ( DOID:0080353 )
- is a type of
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