FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term Noonan syndrome 1 ID (Ontology) DOID:0060578 (Human Disease)
Definition A Noonan syndrome that has_material_basis_in the PTPN11 gene on chromosome 12q24.
Also Known As "NS1"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       6
Human Disease Models (FBhh)  DOID       1
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes Human Disease Models
 Noonan syndrome 1       7      2      1
 for disease ribbon | Noonan syndrome 1       --       1       --
 model of | Noonan syndrome 1       6      1       --
 DOES NOT model | Noonan syndrome 1       1       --       --
Spanning Tree (Parents/Children)
Only view relationship: 
monogenic disease
 |__Noonan syndrome_____________
autosomal genetic disease       |
 |__autosomal dominant disease__|
RASopathy                       |
 |__Noonan syndrome_____________|
                                Noonan syndrome 1  10 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal dominant disease
Noonan syndrome
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "NS1" EXACT OMO:0003012
Secondary IDs
hide External Crossreferences & Linkouts
ICD10CM:Q87.1
MIM:163950