Disease #06507 (OCNDS (Okur-Chung neurodevelopmental syndrome), OMIM:617062)
| Official abbreviation |
OCNDS |
| Name |
Okur-Chung neurodevelopmental syndrome |
| OMIM ID |
617062 |
| 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 |
CSNK2A1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|