isolated growth hormone deficiency, type II

Preferred Label : isolated growth hormone deficiency, type II;

MeSH note : PROM;

MeSH synonym : pituitary dwarfism due to isolated growth hormone deficiency, autosomal dominant; IGHD2; growth hormone deficiency, isolated, autosomal dominant; IGHD II;

Details

Origin ID

C562704;

UMLS CUI

C0271567;

Automatic exact mappings (from CISMeF team)
- Isolated growth hormone deficiency - autosomal dominant (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Isolated growth hormone deficiency type II [ORDO Disease]
- Isolated growth hormone deficiency, type II [OMIM Phenotype]
- isolated growth hormone deficiency type II [DO Concept]
MeSH term(s) associated for indexing
- dwarfism, pituitary [MeSH Descriptor]
Record concept(s)
- isolated growth hormone deficiency, type II [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Isolated growth hormone deficiency - autosomal dominant (disorder) [SNOMED CT concept]
- Isolated growth hormone deficiency type II [ORDO Disease]
- Isolated growth hormone deficiency, type II [OMIM Phenotype]
- autosomal dominant isolated somatotropin deficiency [SNOMED Notion]
- isolated growth hormone deficiency type II [DO Concept]

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