Disease #05962 (NEDAUS (neurodevelopmental disorder with/without autism or seizures), OMIM:619239)
| Official abbreviation |
NEDAUS |
| Name |
neurodevelopmental disorder with/without autism or seizures |
| OMIM ID |
619239 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
CUL3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-08-06 18:44:10 +02:00 (CEST) |
| Date last edited |
2024-12-11 11:24:27 +01:00 (CET) |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|