01
Diseases
Adrenal Hyperplasia, Congenital, Due To 21-Hydroxylase Deficiency
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 17
Basic Information
Grouped by core information, identifiers, and descriptions.
Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
- Disease Name
- Adrenal Hyperplasia, Congenital, Due To 21-Hydroxylase Deficiency
- Standard Disease Name
- adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- No data
- OMIM ID
- 201910
- UMLS ID
- C2936858|C1859995
- HPO ID
- No data
Description and Extensions
- Description
- No data
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Related Targets
target disease1 Targets