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DO Term : Noonan syndrome 3 [DOID:0060581] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Noonan syndrome that has_material_basis_in heterozygous mutation in the KRAS gene.

synonyms:
OMIM:609942,
DOID:0070103,
ICD10CM:Q87.1,
MESH:C537847,
NS3,
609942

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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