Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked

Preferred Label : Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0531610;

UMLS CUI

C0472813;

Currated CISMeF NLP mapping
- Isolated growth hormone deficiency, type III, with agammaglobulinemia [OMIM Phenotype]
- Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia [ORDO Disease]
- X-linked agammaglobulinemia with growth hormone deficiency (disorder) [SNOMED CT concept]
- isolated growth hormone deficiency type III [DO Concept]
Related record
- hypogammaglobulinemia and isolated growth hormone deficiency, X-linked [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Isolated growth hormone deficiency type III [ORDO Disease]
- Isolated growth hormone deficiency, type III, with agammaglobulinemia [OMIM Phenotype]
- Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia [ORDO Disease]
- X-linked agammaglobulinemia with growth hormone deficiency (disorder) [SNOMED CT concept]
- isolated growth hormone deficiency type III [DO Concept]