mental retardation, X-Linked, syndromic 14

Preferred Label : mental retardation, X-Linked, syndromic 14;

MeSH note : mutation in UPF3B;

MeSH synonym : MRXS14;

Origin ID

C567063;

UMLS CUI

C1970822;

Currated CISMeF NLP mapping
- Intellectual developmental disorder, X-linked, syndromic 14 [OMIM Phenotype]
MeSH term(s) associated for indexing
- mental retardation, X-Linked [MeSH Descriptor]
Record concept(s)
- mental retardation, X-Linked, syndromic 14 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Intellectual developmental disorder, X-linked, syndromic 14 [OMIM Phenotype]