Disease #06981 (NOC (neuroocular syndrome), OMIM:619539)
| Official abbreviation |
NOC |
| Name |
neuroocular syndrome |
| OMIM ID |
619539 |
| 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 |
PRR12 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2022-11-30 16:21:49 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|