Disease #05762 (EIEE74 (encephalopathy, epileptic, early infantile, type 74 (EIEE74)), OMIM:618396)
Official abbreviation |
EIEE74 |
Name |
encephalopathy, epileptic, early infantile, type 74 (EIEE74) |
OMIM ID |
618396 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
GABRG2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2020-06-06 18:57:10 +02:00 (CEST) |
Date last edited |
N/A |
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