Any X-linked hypophosphatemic rickets in which the cause of the disease is a mutation in the CLCN5 gene. The disease is Monarch Disease Ontology identifier MONDO_0010358 (hypophosphatemic rickets, X-linked recessive). Also known as: CLCN5 X-linked hypophosphatemic rickets, X-linked hypophosphatemic rickets caused by mutation in CLCN5.