Disease #05407 (FAME1;FMCTE1 (epilepsy, myoclonic, familial adult, type 1 (FAME1, FMCTE1)), OMIM:601068)
| Official abbreviation |
FAME1;FMCTE1 |
| Name |
epilepsy, myoclonic, familial adult, type 1 (FAME1, FMCTE1) |
| OMIM ID |
601068 |
| 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 |
SAMD12 |
| Associated tissues |
- |
| Disease features |
autosomal dominant, benign adult familial myoclonic epilepsy (BAFME) |
| Remarks |
- |
| Date created |
2018-03-18 15:37:28 +01:00 (CET) |
| Date last edited |
2019-12-19 19:05:33 +01:00 (CET) |
Individuals
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