Disease #04645 (ETL7 (epilepsy, temporal lobe, familial, type 7 (ETL-7)), OMIM:616436)

Official abbreviation ETL7
Name epilepsy, temporal lobe, familial, type 7 (ETL-7)
OMIM ID 616436
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene RELN
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00326814 174460 - - F ? Germany - - - - - ETL7 (+) Behavioral abnormality,(+) Eczema,(+) Atopic dermatitis,(+) Seizure,(+) Motor delay,(+) Focal-onset seizure,(+) Delayed fine motor development,(+) Diminished ability to concentrate,(+) Infection-related seizure,(+) Seizure precipitated by febrile infection RELN RELN 1 1 Andreas Laner
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