Disease #03216 (EIEE39 (Epileptic encephalopathy, early infantile, 39), OMIM:612949)
Official abbreviation |
EIEE39 |
Name |
Epileptic encephalopathy, early infantile, 39 |
OMIM ID |
612949 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
SLC25A12 |
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) |
|