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
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