Disease #04537 (DEE32;EIEE32 (encephalopathy, developmental and epileptic, type 32 (DEE32)), OMIM:616366)
| Official abbreviation |
DEE32;EIEE32 |
| Name |
encephalopathy, developmental and epileptic, type 32 (DEE32) |
| OMIM ID |
616366 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
KCNA2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
2022-10-21 09:28:08 +02:00 (CEST) |
Individuals
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