Disease #03049 (EPM3;CLN14 (epilepsy, myoclonic, progressive, type 3 (EPM-3, neuronal ceroid lipofuscinosis, type 14 (CLN-14))), OMIM:611726)
| Official abbreviation |
EPM3;CLN14 |
| Name |
epilepsy, myoclonic, progressive, type 3 (EPM-3, neuronal ceroid lipofuscinosis, type 14 (CLN-14)) |
| OMIM ID |
611726 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
KCTD7 |
| 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.
|