Disease #05441 (NS1 (Noonan syndrome, type 1 (NS1)), OMIM:163950)
| Official abbreviation |
NS1 |
| Name |
Noonan syndrome, type 1 (NS1) |
| OMIM ID |
163950 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
8 |
| Phenotype entries for this disease |
8 |
| Associated with 1 gene |
PTPN11 |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2018-06-20 14:58:17 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|