Disease #02931 (ENFL4 (epilepsy, frontal lobe, nocturnal, type 4 (ENFL-4)), OMIM:610353)
Official abbreviation |
ENFL4 |
Name |
epilepsy, frontal lobe, nocturnal, type 4 (ENFL-4) |
OMIM ID |
610353 |
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 |
CHRNA2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|