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Metadata
ID DOID:0060584
Name Noonan syndrome 6
Definition A Noonan syndrome that has_material_basis_in heterozygous mutation in the NRAS gene on chromosome 1p13.
https://www.ncbi.nlm.nih.gov/pubmed/19966803
Xrefs

ICD10CM:Q87.1

MESH:C548084

OMIM:613224

Alternateids

DOID:0070106

Synonyms

NS6 [EXACT]

Parent Relationships

is_a Noonan syndrome

is_a autosomal dominant disease

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