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MIM:607364 - BARTTER SYNDROME, TYPE 3; BARTS3
Xenbase Genes: clcnkb
Human Disease Resource: MIM
| MONDO:0011822 - dense irregular connective tissue |
| MONDO:0015231 - Bartter syndrome |
| DOID:0110144 - Bartter disease type 3 |
|
| MONDO:0011822 - dense irregular connective tissue |
| MONDO:0015231 - Bartter syndrome |
| DOID:0110144 - Bartter disease type 3 |