ZFIN Human Disease: Noonan syndrome 4

OBO ID: DOID:0060582

OBO ID: DOID:0060582

Term Name:	Noonan syndrome 4	Search Ontology:
Synonyms:	NS4
Definition:	A Noonan syndrome that has_material_basis_in heterozygous mutation in the SOS1 gene on chromosome 2p22. https://www.ncbi.nlm.nih.gov/pubmed/19438935
References:	ICD10CM:Q87.1 MESH:C548082 OMIM:610733
Ontology:	Human Disease ( DOID:0060582 )

Relationships

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

OTHER Noonan syndrome 4 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SOS1	sos1	Noonan syndrome 4	610733

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None