Disease #06586 (EIEE73 (Epileptic encephalopathy, early infantile, 73), OMIM:618379)
Official abbreviation |
EIEE73 |
Name |
Epileptic encephalopathy, early infantile, 73 |
OMIM ID |
618379 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
RNF13 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
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