MCID: PRK015

Park7-Related Parkinson Disease malady

Genetic diseases, Rare diseases, Neuronal diseases, Metabolic diseases, Cancer diseases, Cardiovascular diseases, Mental diseases categories

Summaries for Park7-Related Parkinson Disease

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MalaCards based summary: Park7-Related Parkinson Disease An important gene associated with Park7-Related Parkinson Disease is PARK7 (parkinson protein 7).

Aliases & Classifications for Park7-Related Parkinson Disease

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Park7-Related Parkinson Disease, Aliases & Descriptions:

Name: Park7-Related Parkinson Disease 20


Classifications:



Symptoms for Park7-Related Parkinson Disease

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Drugs & Therapeutics for Park7-Related Parkinson Disease

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Drug clinical trials:

Search ClinicalTrials for Park7-Related Parkinson Disease

Search NIH Clinical Center for Park7-Related Parkinson Disease

Genetic Tests for Park7-Related Parkinson Disease

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Genetic tests related to Park7-Related Parkinson Disease:

id Genetic test Affiliating Genes
1 Park7-Related Parkinson Disease20 PARK7

Anatomical Context for Park7-Related Parkinson Disease

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Animal Models for Park7-Related Parkinson Disease or affiliated genes

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Publications for Park7-Related Parkinson Disease

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Variations for Park7-Related Parkinson Disease

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Expression for genes affiliated with Park7-Related Parkinson Disease

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Search GEO for disease gene expression data for Park7-Related Parkinson Disease.

Pathways for genes affiliated with Park7-Related Parkinson Disease

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Compounds for genes affiliated with Park7-Related Parkinson Disease

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GO Terms for genes affiliated with Park7-Related Parkinson Disease

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Products for genes affiliated with Park7-Related Parkinson Disease

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  • Antibodies
  • Proteins
  • Lysates
  • Antibodies
  • Proteins
  • Kits and Assays

Sources for Park7-Related Parkinson Disease

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3CDC
13ExPASy
14FMA
22GTR
23HGMD
24HMDB
25ICD10
26ICD10 via Orphanet
27ICD9CM
28IUPHAR
29KEGG
33MeSH
34MESH via Orphanet
35MGI
38NCIt
39NDF-RT
42NINDS
43Novoseek
45OMIM
46OMIM via Orphanet
50PubMed
51QIAGEN
56SNOMED-CT via Orphanet
60UMLS
61UMLS via Orphanet