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Metadata
ID DOID:0060588
Name Noonan syndrome 10
Definition A Noonan syndrome that has_material_basis_in heterozygous mutation in the LZTR1 gene on chromosome 22q11.
https://www.ncbi.nlm.nih.gov/pubmed/25795793
Xrefs

ICD10CM:Q87.1

OMIM:616564

Alternateids

DOID:0070110

Synonyms

NS10 [EXACT]

Parent Relationships

is_a Noonan syndrome

is_a autosomal dominant disease

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