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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