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Collaborative Research
Diseases
All human diseases in the Mondo ontology. Any disease or group can have projects.
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23 matches for “Parkinson disease”
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Disease
ID
Subtypes
Genes
Parkinson disease 10
MONDO:0011737
Parkinson disease 12
MONDO:0010360
Parkinson disease 17
MONDO:0013625
VPS35
Parkinson disease 21
MONDO:0014604
Parkinson disease 19B, early-onset
MONDO:0800369
Parkinson disease 3, autosomal dominant
MONDO:0011220
Parkinson disease 22, autosomal dominant
MONDO:0014742
CHCHD2
Late-onset Parkinson disease
MONDO:0008199
7
Young-onset Parkinson disease
MONDO:0017279
13
Early-onset Parkinson disease 20
MONDO:0014233
SYNJ1
Juvenile-onset Parkinson disease
MONDO:0000828
4
Postencephalitic Parkinson disease
MONDO:0001945
Juvenile onset Parkinson disease 19A
MONDO:0014231
DNAJC6
Autosomal dominant Parkinson disease 1
MONDO:0008200
SNCA
Autosomal dominant Parkinson disease 4
MONDO:0011562
SNCA
Autosomal dominant Parkinson disease 8
MONDO:0011764
LRRK2
Autosomal recessive Parkinson disease 14
MONDO:0013060
Autosomal recessive juvenile Parkinson disease 2
MONDO:0010820
PRKN
Autosomal recessive early-onset Parkinson disease 6
MONDO:0011613
PINK1
Autosomal recessive early-onset Parkinson disease 7
MONDO:0011658
PARK7
Autosomal recessive early-onset Parkinson disease 23
MONDO:0014796
VPS13C
Kufor-Rakeb syndrome
MONDO:0011706
1
ATP13A2
Parkinsonian-pyramidal syndrome
MONDO:0009830
1
FBXO7