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Summary Literature (1)
MIM:300554 - HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE

Xenbase Genes: clcn5

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010225 - Dent disease type 1
MONDO:0010358 - hypophosphatemic rickets, X-linked recessive
MONDO:0015612 - Dent disease

Disease Ontology (DO):
DOID:0050445 - X-linked dominant hypophosphatemic rickets