Epilepsy, idiopathic generalized, susceptibility to, 18

Preferred Label : Epilepsy, idiopathic generalized, susceptibility to, 18;

Symbol : EIG18;

Type : Phenotype, molecular basis known;

Prefixed ID : #619521;

Details

Origin ID

619521;

UMLS CUI

C5561983;

Genes related to phenotype
- Hyperpolarization-activated cyclic nucleotide-gated potassium channel 4 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Bradycardia [HPO term]
- Delayed speech and language development [HPO term]
- Infantile onset [HPO term]
- Intellectual disability, mild [HPO term]
- Myoclonic seizure [HPO term]
Semantic type(s)
- Finding [UMLS semantic type]

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