Non-Classic Congenital Adrenal Hyperplasia

Preferred Label : Non-Classic Congenital Adrenal Hyperplasia;

NCIt related terms : Late-onset Congenital Adrenal Hyperplasia;

Alternative definition : NICHD: A milder form of congenital adrenal hyperplasia characterized by decreased activity of an enzyme in the steroidogenic pathway, typically presenting later in life, that does not require life-long cortisol replacement.;

Details

Origin ID

C131442;

UMLS CUI

C0342467;

Automatic exact mappings (from CISMeF team)
- Late onset congenital adrenal hyperplasia (disorder) [SNOMED CT concept]
- Late-onset congenital adrenal hyperplasia [MeSH concept]
- congenital adrenal hyperplasia due to 21 hydroxylase deficiency [MeSH Supplementary Concept]
Has associated anatomic sites
- Adrenal Gland [NCIt concept]
- Peritoneum and Retroperitoneum [NCIt concept]
- Retroperitoneum [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Late onset congenital adrenal hyperplasia (disorder) [SNOMED CT concept]
- Late-onset congenital adrenal hyperplasia [MeSH concept]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Endocrinology Terminology [NCIt concept]
disease_has_primary_anatomic_site
- Adrenal Gland [NCIt concept]
- Peritoneum and Retroperitoneum [NCIt concept]
- Retroperitoneum [NCIt concept]

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