Rolandic epilepsy, mental retardation, and speech dyspraxia, autosomaldominant

Preferred Label : Rolandic epilepsy, mental retardation, and speech dyspraxia, autosomaldominant;

Obsolete resource : true;

Moved to : 245570;

Alternative titles and symbols : Resdad; Adresd;

Description : See also X-linked rolandic epilepsy with speech dyspraxia (RESDX; 300643), caused by mutation in the SRPX2 gene (300642).;

Inheritance : Autosomal dominant;

Prefixed ID : 601085;

Details

Origin ID

601085;

Automatic exact mappings (from CISMeF team)
- Rolandic epilepsy-speech dyspraxia syndrome [ORDO Disease]
Broader ORDO disease(s)
- Rolandic epilepsy-speech dyspraxia syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- rolandic epilepsy, mental retardation, and speech dyspraxia, autosomal dominant [MeSH Supplementary Concept]
HPO term(s)
- Epilepsy [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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