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Hypophosphatemic rickets, X-linked recessive
rareAny X-linked hypophosphatemic rickets in which the cause of the disease is a mutation in the CLCN5 gene.
- Identifiers
- MONDO:0010358 OMIM:300554
- Causal genes
- CLCN5
- Also known as
- CLCN5 X-linked hypophosphatemic rickets · X-linked hypophosphatemic rickets caused by mutation in CLCN5
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