autosomal dominant nocturnal frontal lobe epilepsy 3
autosomal dominant nocturnal frontal lobe epilepsy that has material basis in heterozygous mutation in the CHRNB2 gene on chromosome 1q21
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autosomal dominant nocturnal frontal lobe epilepsy 3
Summary
autosomal dominant nocturnal frontal lobe epilepsy 3 is a rare disease[1].
Key Facts
- autosomal dominant nocturnal frontal lobe epilepsy 3's instance of is recorded as rare disease[2].
- autosomal dominant nocturnal frontal lobe epilepsy 3's instance of is recorded as class of disease[3].
- autosomal dominant nocturnal frontal lobe epilepsy 3's subclass of is recorded as autosomal dominant nocturnal frontal lobe epilepsy[4].
- autosomal dominant nocturnal frontal lobe epilepsy 3's MeSH descriptor ID is recorded as C565334[5].
- autosomal dominant nocturnal frontal lobe epilepsy 3's OMIM ID is recorded as 605375[6].
- autosomal dominant nocturnal frontal lobe epilepsy 3's Disease Ontology ID is recorded as DOID:0060684[7].
- autosomal dominant nocturnal frontal lobe epilepsy 3's genetic association is recorded as CHRNB2[8].
- autosomal dominant nocturnal frontal lobe epilepsy 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060684[9].
- autosomal dominant nocturnal frontal lobe epilepsy 3's exact match is recorded as http://identifiers.org/doid/DOID:0060684[10].
- autosomal dominant nocturnal frontal lobe epilepsy 3's UMLS CUI is recorded as C1854335[11].
- autosomal dominant nocturnal frontal lobe epilepsy 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- autosomal dominant nocturnal frontal lobe epilepsy 3's Mondo ID is recorded as MONDO_0011545[13].
- autosomal dominant nocturnal frontal lobe epilepsy 3's UniProt disease ID is recorded as DI-00820[14].