OBO ID: DOID:0060898 |
Term Name: | Parkinson's disease 20 | Search Ontology: | |
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Definition: | An early-onset Parkinson disease that has_material_basis_in homozygous mutation in the SYNJ1 gene on chromosome 21q22. (2) | ||
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Ontology: | Human Disease ( DOID:0060898 ) |
OTHER Parkinson's disease 20 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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