ZFIN Human Disease: Noonan syndrome 3

OBO ID: DOID:0060581

Term Name:	Noonan syndrome 3		Search Ontology:
Synonyms:	NS3
Definition:	A Noonan syndrome that has_material_basis_in heterozygous mutation in the KRAS gene. https://www.ncbi.nlm.nih.gov/pubmed/16474405
References:	ICD10CM:Q87.1 MESH:C537847 OMIM:609942
Ontology:	Human Disease ( DOID:0060581 )

Relationships

is a type of:	autosomal dominant disease Noonan syndrome autosomal dominant disease Noonan syndrome Show first 5 Terms

OTHER Noonan syndrome 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
KRAS	kras	Noonan syndrome 3	609942

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None