OBO ID: DOID:0060372
Term Name: Parkinson's disease 15 Search Ontology:
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
is a type of:
OTHER Parkinson's disease 15 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FBXO7 Parkinson disease 15, autosomal recessive 260300
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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