PARK12
MCID: PRK022
MIFTS: 17

Parkinson Disease 12 (PARK12)

Categories: Eye diseases, Genetic diseases, Mental diseases, Metabolic diseases, Muscle diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Parkinson Disease 12

MalaCards integrated aliases for Parkinson Disease 12:

Name: Parkinson Disease 12 57 29 13 70
Parkinson Disease, X-Linked 57
Park12 57

Classifications:



External Ids:

OMIM® 57 300557
OMIM Phenotypic Series 57 PS168600
UMLS 70 C1845165

Summaries for Parkinson Disease 12

MalaCards based summary : Parkinson Disease 12, also known as parkinson disease, x-linked, is related to parkinson disease, late-onset and movement disease. An important gene associated with Parkinson Disease 12 is PARK12 (Parkinson Disease 12 (Susceptibility)). Affiliated tissues include cortex.

More information from OMIM: 300557 PS168600

Related Diseases for Parkinson Disease 12

Symptoms & Phenotypes for Parkinson Disease 12

Clinical features from OMIM®:

300557 (Updated 05-Apr-2021)

Drugs & Therapeutics for Parkinson Disease 12

Search Clinical Trials , NIH Clinical Center for Parkinson Disease 12

Genetic Tests for Parkinson Disease 12

Genetic tests related to Parkinson Disease 12:

# Genetic test Affiliating Genes
1 Parkinson Disease 12 29

Anatomical Context for Parkinson Disease 12

MalaCards organs/tissues related to Parkinson Disease 12:

40
Cortex

Publications for Parkinson Disease 12

Articles related to Parkinson Disease 12:

(show all 12)
# Title Authors PMID Year
1
Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families. 57
12925570 2003
2
A susceptibility gene for late-onset idiopathic Parkinson's disease. 57
12402251 2002
3
Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations. 57
12058349 2002
4
Complete genomic screen in Parkinson disease: evidence for multiple genes. 57
11710888 2001
5
Early-onset parkinsonism in a pedigree with phosphoglycerate kinase deficiency and a heterozygous carrier: do PGK-1 mutations contribute to vulnerability to parkinsonism? 61
28649613 2017
6
Neuroimmunology of the Interleukins 13 and 4. 61
27304970 2016
7
Consistency in Administration and Response for the Backward Push and Release Test: A Clinical Assessment of Postural Responses. 61
25431128 2016
8
Genetic analysis of the ATP1B4 gene in Chinese Han patients with Parkinson's disease. 61
24420862 2014
9
Cutting edge: IL-13Rα1 expression in dopaminergic neurons contributes to their oxidative stress-mediated loss following chronic peripheral treatment with lipopolysaccharide. 61
23169588 2012
10
Motor cortex stimulation in patients with Parkinson disease: 12-month follow-up in 4 patients. 61
18590444 2008
11
Genetics of Parkinson's disease and parkinsonism. 61
17068789 2006
12
Reliability of physical performance tests in four different randomized clinical trials. 61
10326921 1999

Variations for Parkinson Disease 12

Expression for Parkinson Disease 12

Search GEO for disease gene expression data for Parkinson Disease 12.

Pathways for Parkinson Disease 12

GO Terms for Parkinson Disease 12

Sources for Parkinson Disease 12

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 05-Apr-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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