ZFIN Human Disease: Parkinson's disease 23

OBO ID: DOID:0060896

Term Name:	Parkinson's disease 23		Search Ontology:
Synonyms:	autosomal recessive early-onset Parkinson disease 23 autosomal recessive early-onset Parkinson's disease 23
Definition:	An early-onset Parkinson disease that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22. https://www.ncbi.nlm.nih.gov/pubmed/26942284
References:	ICD10CM:G20 OMIM:616840
Ontology:	Human Disease ( DOID:0060896 )

Relationships

is a type of:	autosomal recessive disease early-onset Parkinson's disease autosomal recessive disease early-onset Parkinson's disease Show first 5 Terms

OTHER Parkinson's disease 23 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
VPS13C	vps13c	Parkinson disease 23, autosomal recessive, early onset	616840

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None