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MIM:310468 - NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE; XRN
Xenbase Genes: clcn5
Human Disease Resource: OMIM
MONDO:0010225 - Dent disease type 1 |
MONDO:0010687 - nephrolithiasis, X-linked recessive, with renal failure |
MONDO:0015612 - Dent disease |
DOID:0111798 - X-linked nephrolithiasis type I |