Disease #05854 (NS2 (Noonan syndrome, type 2 (NS2)), OMIM:605275)
| Official abbreviation |
NS2 |
| Name |
Noonan syndrome, type 2 (NS2) |
| OMIM ID |
605275 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
LZTR1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-10-16 09:46:56 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|