Noonan syndrome 6

Summary
Synonym
  • NS6
Definition
A Noonan syndrome that has_material_basis_in heterozygous mutation in the NRAS gene on chromosome 1p13.
Super Class
Noonan syndrome autosomal dominant disease
Disease Ontology
DOID:0060584
Mondo Disease Ontology
MeSH
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4893 NRAS NRAS proto-oncogene, GTPase
The Human Phenotype Ontology
Displaying entries 91 - 96 of 96 in total
HPO ID HPO Term
HP:0006889 Intellectual disability, borderline
HP:0001561 Polyhydramnios
HP:0011968 Feeding difficulties
HP:0001642 Pulmonic stenosis
HP:0001488 Bilateral ptosis
HP:0004523 Long eyebrows
Displaying all 2 entries
Gene ID Gene Symbol Description
3845 KRAS KRAS proto-oncogene, GTPase
4893 NRAS NRAS proto-oncogene, GTPase

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024