Disease #00682 (NS3 (Noonan syndrome, type 3 (NS-3)), OMIM:609942)
Official abbreviation |
NS3 |
Name |
Noonan syndrome, type 3 (NS-3) |
OMIM ID |
609942 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
KRAS |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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