pituitary hormone deficiency, combined, 2

Preferred Label : pituitary hormone deficiency, combined, 2;

MeSH note : PROM mutation in PROP1;

MeSH synonym : pituitary dwarfism III; ateliotic dwarfism with hypogonadism; hanhart dwarfism;

Details

Origin ID

C563172;

UMLS CUI

C0878683;

Currated CISMeF NLP mapping
- Pituitary hormone deficiency, combined, 2 [OMIM Phenotype]
MeSH term(s) associated for indexing
- dwarfism, pituitary [MeSH Descriptor]
Record concept(s)
- pituitary hormone deficiency, combined, 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Pituitary hormone deficiency, combined, 2 [OMIM Phenotype]

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