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Metadata
ID DOID:0060585
Name Noonan syndrome 7
Definition A Noonan syndrome that has_material_basis in heterozygous mutation in the BRAF gene.
https://www.ncbi.nlm.nih.gov/pubmed/19206169
Xrefs

ICD10CM:Q87.1

OMIM:613706

Alternateids

DOID:0070107

Synonyms

NS7 [EXACT]

Parent Relationships

is_a Noonan syndrome

is_a autosomal dominant disease

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