Disease #00097 (FIME (epilepsy, myoclonic, infantile, familial (FIME)), OMIM:605021)
Official abbreviation |
FIME |
Name |
epilepsy, myoclonic, infantile, familial (FIME) |
OMIM ID |
605021 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
TBC1D24 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2012-12-14 10:00:34 +01:00 (CET) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|