Hypoaldosteronism, congenital, due to CMO II deficiency

Test Type : Molecular
Test Name : Hypoaldosteronism, congenital, due to CMO II deficiency
Gene Name : CYP11B2
OMIM No : 124080
Phenotype Number : 610600
LOKASYON GRCh38 : 8:142,910,558-142,917,842
Sample Type : EDTA BLOOD
Result Time : 45-60 Day
Type of Transfer : 4° / 30°
SUT Code : G100390
Transaction Name : Next Generation DNA Sequencing, 1 Gen
Method : Sequencing
Ref SEQ : NM_000498
Other informations :