Disease #05435 (DEE92;IECEE2 (encephalopathy, developmental and epileptic, type92 (IECEE2)), OMIM:617829)
Official abbreviation |
DEE92;IECEE2 |
Name |
encephalopathy, developmental and epileptic, type92 (IECEE2) |
OMIM ID |
617829 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
GABRB2 |
Associated tissues |
- |
Disease features |
autosomal dominant |
Remarks |
- |
Date created |
2018-06-01 14:38:04 +02:00 (CEST) |
Date last edited |
2023-10-23 12:25:49 +02:00 (CEST) |
Individuals
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