mental retardation, X-Linked, with isolated growth hormone deficiency

Preferred Label : mental retardation, X-Linked, with isolated growth hormone deficiency;

Origin ID

C564712;

UMLS CUI

C1848068;

Automatic exact mappings (from CISMeF team)
- Intellectual developmental disorder, X-linked, with panhypopituitarism [OMIM Phenotype]
MeSH term(s) associated for indexing
- dwarfism, pituitary [MeSH Descriptor]
- mental retardation, X-Linked [MeSH Descriptor]
Record concept(s)
- mental retardation, X-Linked, with isolated growth hormone deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- X-linked intellectual disability with isolated growth hormone deficiency [ORDO Disease]