Disease #04390 (EIEE50 (encephalopathy, epileptic, early infantile,, type 50 (EIEE-50)), OMIM:616457)
Official abbreviation |
EIEE50 |
Name |
encephalopathy, epileptic, early infantile,, type 50 (EIEE-50) |
OMIM ID |
616457 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
CAD |
Associated tissues |
- |
Disease features |
autosomal recessive |
Remarks |
- |
Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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