ZFIN Human Disease: Parkinson's disease 22

OBO ID: DOID:0080504

Term Name:	Parkinson's disease 22		Search Ontology:
Synonyms:	autosomal dominant Parkinson's disease 22
Definition:	A late onset Parkinson's disease that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the coiled-coil-helix-coiled-coil-helix domain containing 2 gene on chromosome 7p11.2. (2)
References:	OMIM:616710
Ontology:	Human Disease ( DOID:0080504 )

Relationships

is a type of:	autosomal dominant disease late onset Parkinson's disease autosomal dominant disease late onset Parkinson's disease Show first 5 Terms

OTHER Parkinson's disease 22 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CHCHD2	chchd2	Parkinson disease 22, autosomal dominant	616710

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None