pituitary hormone deficiency, combined, 1

Preferred Label : pituitary hormone deficiency, combined, 1;

MeSH note : also known as CPHD1;

Origin ID

C567803;

UMLS CUI

C2751608;

Currated CISMeF NLP mapping
- Pituitary hormone deficiency, combined or isolated, 1 [OMIM Phenotype]
MeSH term(s) associated for indexing
- abnormalities, multiple [MeSH Descriptor]
- facies [MeSH Descriptor]
- hypothyroidism [MeSH Descriptor]
- pituitary hormones, anterior [MeSH Descriptor]
- transcription factor pit-1 [MeSH Descriptor]
Record concept(s)
- pituitary hormone deficiency, combined, 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Pituitary hormone deficiency, combined or isolated, 1 [OMIM Phenotype]