familial temporal lobe epilepsy 7
temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has material basis in heterozygous mutation in the RELN gene on chromosome 7q22
Press Enter · cited answer in seconds
0 sources
familial temporal lobe epilepsy 7
Summary
familial temporal lobe epilepsy 7 is a class of disease[1].
Key Facts
- familial temporal lobe epilepsy 7's instance of is recorded as class of disease[2].
- familial temporal lobe epilepsy 7's subclass of is recorded as temporal lobe epilepsy[3].
- familial temporal lobe epilepsy 7's subclass of is recorded as genetic disease[4].
- familial temporal lobe epilepsy 7's subclass of is recorded as familial partial epilepsy[5].
- familial temporal lobe epilepsy 7's subclass of is recorded as autosomal dominant disease[6].
- familial temporal lobe epilepsy 7's OMIM ID is recorded as 616436[7].
- familial temporal lobe epilepsy 7's Disease Ontology ID is recorded as DOID:0060751[8].
- familial temporal lobe epilepsy 7's Orphanet ID is recorded as 101046[9].
- familial temporal lobe epilepsy 7's genetic association is recorded as RELN[10].
- familial temporal lobe epilepsy 7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060751[11].
- familial temporal lobe epilepsy 7's exact match is recorded as http://identifiers.org/doid/DOID:0060751[12].
- familial temporal lobe epilepsy 7's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101046[13].
- familial temporal lobe epilepsy 7's UMLS CUI is recorded as C4225327[14].
- familial temporal lobe epilepsy 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- familial temporal lobe epilepsy 7's Mondo ID is recorded as MONDO_0014639[16].
- familial temporal lobe epilepsy 7's UniProt disease ID is recorded as DI-04463[17].