21-hydroxylase deficiency

Symptom Information:

Symptom ID: MedDRA:10000021
Synonyms:
21-hydroxylase deficiency [OMIM:21-hydroxylase deficiency]
Quality:
Cross references:
OMIM: "21-hydroxylase deficiency" [OMIM:21-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)
          21-hydroxylase deficiency(MedDRA:10000021)
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (Orphanet:90794)