|OBO ID: DOID:0080504|
|Term Name:||Parkinson's disease 22||Search Ontology:|
|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)|
|Ontology:||Human Disease (DOID:0080504)|
|is a type of:||
OTHER Parkinson's disease 22 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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