Disease #05440 (NS9 (Noonan syndrome, type 9 (NS-9)), OMIM:616559)
| Official abbreviation |
NS9 |
| Name |
Noonan syndrome, type 9 (NS-9) |
| OMIM ID |
616559 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
SOS2 |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2018-06-20 14:52:07 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|