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DO Term : Noonan syndrome 10 [DOID:0060588] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Noonan syndrome that has_material_basis_in heterozygous mutation in the LZTR1 gene on chromosome 22q11.

synonyms:
DOID:0070110,
NS10,
616564,
OMIM:616564,
ICD10CM:Q87.1

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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