premature ovarian failure 2b

Preferred Label : premature ovarian failure 2b;

MeSH note : aks POF2b; associated with mutations in POF1B;

Origin ID

C564476;

UMLS CUI

C1845105;

Currated CISMeF NLP mapping
- Premature ovarian failure 2b [OMIM Phenotype]
MeSH term(s) associated for indexing
- primary ovarian insufficiency [MeSH Descriptor]
Record concept(s)
- premature ovarian failure 2b [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Premature ovarian failure 2b [OMIM Phenotype]