Disease #04411 (ENFL1 (epilepsy, frontal lobe, nocturnal, type 1 (ENFL-1)), OMIM:600513)
Official abbreviation |
ENFL1 |
Name |
epilepsy, frontal lobe, nocturnal, type 1 (ENFL-1) |
OMIM ID |
600513 |
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 |
CHRNA4 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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