Disease #00564 (NS4 (Noonan syndrome, type 4 (NS-4)), OMIM:610733)
Official abbreviation |
NS4 |
Name |
Noonan syndrome, type 4 (NS-4) |
OMIM ID |
610733 |
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 |
SOS1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
|