OBO ID: DOID:0080504
Term Name: Parkinson's disease 22 Search Ontology:
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)
OTHER Parkinson's disease 22 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CHCHD2 Parkinson disease 22, autosomal dominant 616710
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None