ZFIN Human Disease: Noonan syndrome 8

OBO ID: DOID:0060586

OBO ID: DOID:0060586

Term Name:	Noonan syndrome 8	Search Ontology:
Synonyms:	NS8
Definition:	A Noonan syndrome that has_material_basis_in caused by heterozygous mutation in the RIT1 gene on chromosome 1q22. (2)
References:	ICD10CM:Q87.1 OMIM:615355
Ontology:	Human Disease ( DOID:0060586 )

Relationships

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

OTHER Noonan syndrome 8 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
RIT1	rit1	Noonan syndrome 8	615355

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None