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Human Disease

Parkinson's disease 15

Term ID
DOID:0060372
Synonyms
  • autosomal recessive early-onset Parkinson disease 15
  • autosomal recessive early-onset Parkinson's disease 15
  • pallidopyramidal syndrome
  • Parkinsonian-pyramidal syndrome
Definition
An early-onset Parkinson's disease that has_material_basis_in mutation in the FBXO7 gene on chromosome 22q12.3. https://www.ncbi.nlm.nih.gov/pubmed/22315721
References
Ontology
Human Disease   ( DOID:0060372 )
Relationships
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Genes Involved
Zebrafish Models