ZFIN Human Disease: Cornelia de Lange syndrome 3

OBO ID: DOID:0080507

Term Name:	Cornelia de Lange syndrome 3		Search Ontology:
Synonyms:	CDLS3 Cornelia De Lange syndrome 3 with or without midline brain defects
Definition:	A Cornelia de Lange syndrome that has_material_basis_in heterozygous mutation in the SMC3 gene on chromosome 10q25.2. https://www.ncbi.nlm.nih.gov/pubmed/25655089
References:	OMIM:610759
Ontology:	Human Disease ( DOID:0080507 )

Relationships

is a type of:	autosomal dominant disease Cornelia de Lange syndrome autosomal dominant disease Cornelia de Lange syndrome Show first 5 Terms

OTHER Cornelia de Lange syndrome 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SMC3	smc3	Cornelia de Lange syndrome 3	610759

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None