Hypophosphatemic rickets, X-linked recessive

MONDO:0010358

Any X-linked hypophosphatemic rickets in which the cause of the disease is a mutation in the CLCN5 gene.

Also known as: CLCN5 X-linked hypophosphatemic rickets, X-linked hypophosphatemic rickets caused by mutation in CLCN5, hypophosphatemic rickets, X-linked recessive

35 clinical trials for this condition and its sub-types.

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