Disease #05950 (NEDBA (neurodevelopmental disorder with/without variable brain abnormalities (NEDBA)), OMIM:618443)
| Official abbreviation |
NEDBA |
| Name |
neurodevelopmental disorder with/without variable brain abnormalities (NEDBA) |
| OMIM ID |
618443 |
| 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 |
MAPK8IP3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-06-23 17:23:30 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|