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Human Disease

Parkinson's disease 23

Term ID
DOID:0060896
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
Ontology
Human Disease   ( DOID:0060896 )
Relationships
is a type of
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Genes Involved
Zebrafish Models