adrenal hypoplasia, congenital, with precocious puberty

Preferred Label : adrenal hypoplasia, congenital, with precocious puberty;

MeSH note : mutation in NR0B1;

MeSH synonym : adrenal insufficiency, progressive, and hypogonadotropic hypogonadism;

Details

Origin ID

C564568;

UMLS CUI

C1846220;

MeSH term(s) associated for indexing
- adrenal hyperplasia, congenital [MeSH Descriptor]
- genetic diseases, X-linked [MeSH Descriptor]
- puberty, precocious [MeSH Descriptor]
Record concept(s)
- adrenal hypoplasia, congenital, with precocious puberty [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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