autosomal dominant nocturnal frontal lobe epilepsy 5
autosomal dominant nocturnal frontal lobe epilepsy that has material basis in heterozygous mutation in the KCNT1 gene on chromosome 9q34
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autosomal dominant nocturnal frontal lobe epilepsy 5
Summary
autosomal dominant nocturnal frontal lobe epilepsy 5 is a class of disease[1].
Key Facts
- autosomal dominant nocturnal frontal lobe epilepsy 5's instance of is recorded as class of disease[2].
- autosomal dominant nocturnal frontal lobe epilepsy 5's subclass of is recorded as autosomal dominant nocturnal frontal lobe epilepsy[3].
- autosomal dominant nocturnal frontal lobe epilepsy 5's OMIM ID is recorded as 615005[4].
- autosomal dominant nocturnal frontal lobe epilepsy 5's Disease Ontology ID is recorded as DOID:0060686[5].
- autosomal dominant nocturnal frontal lobe epilepsy 5's genetic association is recorded as KCNT1[6].
- autosomal dominant nocturnal frontal lobe epilepsy 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060686[7].
- autosomal dominant nocturnal frontal lobe epilepsy 5's exact match is recorded as http://identifiers.org/doid/DOID:0060686[8].
- autosomal dominant nocturnal frontal lobe epilepsy 5's UMLS CUI is recorded as C3554306[9].
- autosomal dominant nocturnal frontal lobe epilepsy 5's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].
- autosomal dominant nocturnal frontal lobe epilepsy 5's Mondo ID is recorded as MONDO_0014002[11].
- autosomal dominant nocturnal frontal lobe epilepsy 5's UniProt disease ID is recorded as DI-03663[12].