ZFIN Human Disease: Cornelia de Lange syndrome 5

OBO ID: DOID:0080509

Term Name:	Cornelia de Lange syndrome 5		Search Ontology:
Synonyms:
Definition:	A Cornelia de Lange syndrome that has_material_basis_in by mutation in the HDAC8 gene on chromosome Xq13. https://www.ncbi.nlm.nih.gov/pubmed/22889856
References:	OMIM:300882
Ontology:	Human Disease ( DOID:0080509 )

Relationships

is a type of:	Cornelia de Lange syndrome X-linked dominant disease Cornelia de Lange syndrome X-linked dominant disease Show first 5 Terms

OTHER Cornelia de Lange syndrome 5 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
HDAC8	hdac8	Cornelia de Lange syndrome 5	300882

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None