mental retardation, autosomal recessive 13

Preferred Label : mental retardation, autosomal recessive 13;

MeSH note : TRAPPC9 mutations;

MeSH synonym : Mrt13;

Origin ID

C567714;

UMLS CUI

C2750791;

Currated CISMeF NLP mapping
- Intellectual developmental disorder, autosomal recessive 13 [OMIM Phenotype]
MeSH term(s) associated for indexing
- intellectual disability [MeSH Descriptor]
Record concept(s)
- mental retardation, autosomal recessive 13 [MeSH concept]
Semantic type(s)
- Mental or Behavioral Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- Intellectual developmental disorder, autosomal recessive 13 [OMIM Phenotype]