ZFIN Human Disease: Parkinson's disease 6

OBO ID: DOID:0060369

Term Name:	Parkinson's disease 6		Search Ontology:
Synonyms:	autosomal recessive early-onset Parkinson disease 6 autosomal recessive early-onset Parkinson's disease 6 early-onset Parkinson disease 6
Definition:	An early-onset Parkinson's disease that has_material_basis_in mutations in the PINK1 gene on chromosome 1p36.12. https://www.ncbi.nlm.nih.gov/pubmed/22315721
References:	OMIM:605909
Ontology:	Human Disease (DOID:0060369)

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 6 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
PINK1	pink1	Parkinson disease 6, early onset	605909

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS (1)