Myoclonic epilepsy, hartung type

Preferred Label : Myoclonic epilepsy, hartung type;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant form; also autosomal recessive types;

Prefixed ID : %159600;

Details

Origin ID

159600;

UMLS CUI

C1834581;

Currated CISMeF NLP mapping
- myoclonic epilepsy, hartung type [MeSH concept]
- myoclonic epilepsy, hartung type [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Epilepsy [HPO term]
- Generalized myoclonic seizure [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- myoclonic epilepsy, hartung type [MeSH Supplementary Concept]
- myoclonic epilepsy, hartung type [MeSH concept]

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