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Disease association ontology term - MONDO:0012371 - Noonan syndrome 3

Term summary

ID
MONDO:0012371
Name
Noonan syndrome 3
Ontology or CV name
Disease association
Definition
Any Noonan syndrome in which the cause of the disease is a mutation in the KRAS gene.

Parents

Annotation

Disease association

MONDO:0012371 - Noonan syndrome 3

References:

Genes: