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DO Term : Noonan syndrome 9 [DOID:0060587] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Noonan syndrome that has_material_basis_in heterozygous mutation in the SOS2 gene on chromosome 14q21.

synonyms:
616559,
OMIM:616559,
ICD10CM:Q87.1,
NS9,
DOID:0070109

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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