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MIM:601678 - BARTTER SYNDROME, TYPE 1, ANTENATAL; BARTS1
Xenbase Genes: slc12a1
Human Disease Resource: OMIM
MONDO:0011127 - obsolete Bartter disease type 1 |
MONDO:0015231 - Bartter syndrome |
MONDO:0100344 - Bartter disease type 1 |
DOID:0110142 - Bartter disease type 1 |