ZFIN Human Disease: Noonan syndrome 12

OBO ID: DOID:0112170

Term Name:	Noonan syndrome 12		Search Ontology:
Synonyms:	NS12
Definition:	A Noonan syndrome characterized by macrocephaly, facial anomalies including hypertelorism, downslanting palpebral fissures, and low-set ears, and other Noonan syndrome features that has_material_basis_in heterozygous mutation in the RRAS2 gene on chromosome 11p15.2. (2)
References:	OMIM:618624
Ontology:	Human Disease ( DOID:0112170 )

Relationships

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

OTHER Noonan syndrome 12 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
RRAS2	rras2	Noonan syndrome 12	618624

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None