21-hydroxylase deficiency
Symptom Information:
Symptom ID: | MedDRA:10000021 | ||
Synonyms: |
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Is a (Direct Parents): |
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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) |
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Database Frequency: | 1 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | (Orphanet:90794) |