isolated growth hormone deficiency, type II

Preferred Label : isolated growth hormone deficiency, type II;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0563004;

UMLS CUI

C0271567;

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]
Related record
- isolated growth hormone deficiency, type II [MeSH Supplementary 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]