17-alpha-hydroxylase deficiency

Symptom Information:

Symptom ID: MedDRA:10000014
Synonyms:
17-alpha-hydroxylase deficiency [OMIM:17-alpha-hydroxylase deficiency]
Quality:
Cross references:
OMIM: "17-alpha-hydroxylase deficiency" [OMIM:17-alpha-hydroxylase deficiency]
Is a (Direct Parents):
MedDRA Inborn errors of steroid synthesis
Is a (Whole tree): HPO:
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Metabolic and nutritional disorders congenital(MedDRA:10027424)
       Inborn errors of steroid synthesis(MedDRA:10021608)
          17-alpha-hydroxylase deficiency(MedDRA:10000014)
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency (Orphanet:90793)