ZFIN Human Disease: Noonan syndrome 5

OBO ID: DOID:0060583

Term Name:	Noonan syndrome 5		Search Ontology:
Synonyms:	NS5
Definition:	A Noonan syndrome that has_material_basis_in mutation in the RAF1 gene. https://www.ncbi.nlm.nih.gov/pubmed/17603483
References:	ICD10CM:Q87.1 MESH:C548083 OMIM:611553
Ontology:	Human Disease ( DOID:0060583 )

Relationships

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

OTHER Noonan syndrome 5 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
RAF1	raf1a raf1b	Noonan syndrome 5	611553

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None