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Human Disease

Parkinson's disease 22

Term ID
DOID:0080504
Synonyms
  • autosomal dominant Parkinson's disease 22
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)
References
Ontology
Human Disease   ( DOID:0080504 )
Relationships
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Genes Involved
Zebrafish Models