SHMARQL

familial temporal lobe epilepsy 7

<http://www.wikidata.org/entity/Q3589154>

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
rdfs:label
"familial temporal lobe epilepsy 7"@en
skos:altLabel
"EPILEPSY, FAMILIAL TEMPORAL LOBE, 7"@en
"EPILEPSY, FAMILIAL TEMPORAL LOBE, 7; ETL7"@en
"ETL7"@en
"Epilepsy, Familial Temporal Lobe, type 7"@en
"familial temporal lobe epilepsy type 7"@en
schema:description
"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"@en
schema:dateModified "2026-07-05T11:10:14+00:00"^^xsd:dateTime
schema:version 2514103361
wikibase:identifiers 6
wikibase:sitelinks 1
wikibase:statements 16
p:P11430 wd:statement/Q3589154-3ce4bc87-4a95-8f27-d68e-0afd70d79ba9
p:P1550 wd:statement/Q3589154-be1bb067-45c1-91c5-8142-8ff4aab41396
p:P2293 wd:statement/Q3589154-0B5DFD84-CA21-493B-83A1-D75F33BCE366
p:P279 wd:statement/Q3589154-42f06944-4e9e-9c9d-8d93-290832120238
wd:statement/Q3589154-5C3D1523-B0B4-4927-8CC7-3218CEE2E37D
wd:statement/Q3589154-60A31924-A21B-4852-8441-776AF2C15F83
wd:statement/Q3589154-D66FCDAC-F2C5-4AF0-B955-E28258139FB8
p:P2888 wd:statement/Q3589154-0A3CAC5B-1A62-41DB-98EF-4DFE541E5CE6
wd:statement/Q3589154-0F32A34E-5620-4974-A481-EDADAD78DC6A
wd:statement/Q3589154-1B27B98A-6A99-425C-9073-30310E416B5A
p:P2892 wd:statement/Q3589154-D016A2A4-9EE2-45B6-B5B3-A4C99925DE47
p:P31 wd:statement/Q3589154-C611EA7A-68F1-4EF2-B6C1-5BA1077227FB
p:P492 wd:statement/Q3589154-B8C4A73C-0344-49FC-90CB-07E86FE21ED7
p:P5008 wd:statement/Q3589154-536C1390-62F8-4361-B4C5-099EF8B14731
p:P5270 wd:statement/Q3589154-59024B51-16AE-4BEA-BC37-F1FBDEB48C8A
p:P699 wd:statement/Q3589154-B69E12B2-1185-4C84-BE1E-A0AA01DFFF41
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0014639>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0060751>
wdt:P11430 "DI-04463"
wdt:P1550 "101046"
wdt:P2293 RELN
wdt:P279 autosomal dominant disease
familial partial epilepsy
temporal lobe epilepsy
wdt:P2888 <http://identifiers.org/doid/DOID:0060751>
<http://purl.obolibrary.org/obo/DOID_0060751>
<http://www.orpha.net/ORDO/Orphanet_101046>
wdt:P2892 "C4225327"
wdt:P31 type of disease
wdt:P492 "616436"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0014639"
wdt:P699 "DOID:0060751"
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