View disease #00030

Official abbreviation CAH1
Name ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY
OMIM ID 201910
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CYP21A2

  Powered by LOVD v.3.0 Build 16
LOVD software ©2004-2016 Leiden University Medical Center