Disease #00283 (EIEE16 (encephalopathy, epileptic, early infantile, type 16 (EIEE-16)), OMIM:615338)
Official abbreviation |
EIEE16 |
Name |
encephalopathy, epileptic, early infantile, type 16 (EIEE-16) |
OMIM ID |
615338 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
TBC1D24 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2013-11-28 15:56:49 +01:00 (CET) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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