late onset Parkinson's disease

Summary
Synonym
  • late onset Parkinson disease
Definition
A Parkinson's disease characterized by onset of motor symptoms typically after 60 years of age.
Super Class
Parkinson's disease
Disease Ontology
DOID:0060892
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying entries 1 - 10 of 12 in total
Gene ID Gene Symbol Description Source
126 ADH1C alcohol dehydrogenase 1C (class I), gamma polypeptide
1981 EIF4G1 eukaryotic translation initiation factor 4 gamma 1
2629 GBA1 glucosylceramidase beta 1
3122 HLA-DRA major histocompatibility complex, class II, DR alpha
4137 MAPT microtubule associated protein tau
4287 ATXN3 ataxin 3
5660 PSAP prosaposin
6311 ATXN2 ataxin 2
6908 TBP TATA-box binding protein
7384 UQCRC1 ubiquinol-cytochrome c reductase core protein 1
Displaying all 9 entries
Gene ID Gene Symbol Description Source
11522 Adh1 alcohol dehydrogenase 1 (class I)
14466 Gba1 glucosylceramidase beta 1
17762 Mapt microtubule-associated protein tau
19156 Psap prosaposin
20239 Atxn2 ataxin 2
22273 Uqcrc1 ubiquinol-cytochrome c reductase core protein 1
73078 Pmpcb peptidase (mitochondrial processing) beta
208643 Eif4g1 eukaryotic translation initiation factor 4, gamma 1
100504404 H2-Ea histocompatibility 2, class II antigen E alpha
Displaying all 2 entries
Gene ID Gene Symbol Description Source
25524 Psap prosaposin
301011 Uqcrc1 ubiquinol-cytochrome c reductase core protein 1
Displaying all 2 entries
Gene ID Gene Symbol Description Source
41883 Atx2 Ataxin-2
43839 eIF4G1 eukaryotic translation initiation factor 4G1
Displaying all 2 entries
Gene ID Gene Symbol Description Source
177314 gba-4 Putative glucosylceramidase 4
178535 gba-3 Putative glucosylceramidase 3
Displaying all 2 entries
Gene ID Gene Symbol Description Source
852833 TIF4632 translation initiation factor eIF4G
853071 TIF4631 translation initiation factor eIF4G
The Human Phenotype Ontology
Displaying entries 11 - 20 of 29 in total
HPO ID HPO Term
HP:0000738 Hallucinations
HP:0007311 Short stepped shuffling gait
HP:0001332 Dystonia
HP:0002322 Resting tremor
HP:0000006 Autosomal dominant inheritance
HP:0002063 Rigidity
HP:0003587 Insidious onset
HP:0000751 Personality changes
HP:0011960 Substantia nigra gliosis
HP:0001337 Tremor
Displaying all 2 entries
Gene ID Gene Symbol Description
126 ADH1C alcohol dehydrogenase 1C (class I), gamma polypeptide
2629 GBA1 glucosylceramidase beta 1

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Last updated: December 9, 2024