rolandic epilepsy, mental retardation, and speech dyspraxia, X-Linked

Preferred Label : rolandic epilepsy, mental retardation, and speech dyspraxia, X-Linked;

Origin ID

C564467;

UMLS CUI

C1845070;

Currated CISMeF NLP mapping
- Rolandic epilepsy, impaired intellectual development, and speech dyspraxia, X-linked [OMIM Phenotype]
MeSH term(s) associated for indexing
- apraxias [MeSH Descriptor]
- epilepsy, rolandic [MeSH Descriptor]
- genetic diseases, X-linked [MeSH Descriptor]
- intellectual disability [MeSH Descriptor]
- speech disorders [MeSH Descriptor]
Record concept(s)
- rolandic epilepsy, mental retardation, and speech dyspraxia, X-Linked [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Rolandic epilepsy, impaired intellectual development, and speech dyspraxia, X-linked [OMIM Phenotype]