OBO ID: DOID:0080504 |
Term Name: | Parkinson's disease 22 | Search Ontology: | |
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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) | ||
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Ontology: | Human Disease ( DOID:0080504 ) |
OTHER Parkinson's disease 22 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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