Disease #07167 (DEDISB (developmental delay, impaired speech, and behavioral abnormalities, with/without seizures), OMIM:619964)
| Official abbreviation |
DEDISB |
| Name |
developmental delay, impaired speech, and behavioral abnormalities, with/without seizures |
| OMIM ID |
619964 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ARFGEF1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2025-06-19 11:09:47 +02:00 (CEST) |
| Date last edited |
N/A |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|