ZFIN Human Disease: Noonan syndrome 10

OBO ID: DOID:0060588

Term Name:	Noonan syndrome 10		Search Ontology:
Synonyms:	NS10
Definition:	A Noonan syndrome that has_material_basis_in heterozygous mutation in the LZTR1 gene on chromosome 22q11. https://www.ncbi.nlm.nih.gov/pubmed/25795793
References:	ICD10CM:Q87.1 OMIM:616564
Ontology:	Human Disease ( DOID:0060588 )

Relationships

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

OTHER Noonan syndrome 10 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
LZTR1	lztr1	Noonan syndrome 10	616564

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None