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DO Term : Noonan syndrome with multiple lentigines 2 [DOID:0080549] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Noonan syndrome with multiple lentigines that has_material_basis_in heterozygous mutation in the RAF1 gene on chromosome 3p25.

synonyms:
611554,
MESH:C537117,
OMIM:611554,
LEOPARD syndrome 2

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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