help  | about  | cite  | software

Disease :

Primary Identifier  OMIM:202010 Name  ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASE DEFICIENCY

Function

Disease --> HPO phenotype terms

Genomics

1 Genes

Disease

Disease --> HPO phenotype terms

 

Other

18 Alleles

3 Data Sets

21 Publications