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Human Disease

X-linked recessive hypophosphatemic rickets

Term ID
DOID:0080353
Synonyms
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 )
Relationships
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Genes Involved
Zebrafish Models