KCNJ1
Deellabo: | PGD DNA |
Gen (Gen Code): | KCNJ1 |
Aliases Gen: | KIR1.1, ROMK, ROMK1 |
Gen ID (NCBI): | 3758 |
OMIM Gen ID: | 600359 |
Chromosomale locatie: | 11q24 |
Genetische aandoening / Analyse: | Bartter syndroom type 2 |
OMIM aandoening ID: | 241200 |
Overerving: | AR |
Aliases aandoening: | BARTTER SYNDROME, ANTENATAL, TYPE 2 HYPOKALEMIC ALKALOSIS WITH HYPERCALCIURIA, ANTENATAL, 2 HYPERPROSTAGLANDIN E SYNDROME 2 |