MCID: SNC002

Snca-Related Parkinson Disease malady

Genetic diseases, Rare diseases, Neuronal diseases, Eye diseases, Metabolic diseases, Mental diseases categories
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Summaries for Snca-Related Parkinson Disease

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MalaCards based summary: Snca-Related Parkinson Disease An important gene associated with Snca-Related Parkinson Disease is SNCA (synuclein, alpha (non A4 component of amyloid precursor)).

Aliases & Classifications for Snca-Related Parkinson Disease

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Snca-Related Parkinson Disease, Aliases & Descriptions:

Name: Snca-Related Parkinson Disease 20


Classifications:



Symptoms for Snca-Related Parkinson Disease

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Drugs & Therapeutics for Snca-Related Parkinson Disease

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Drug clinical trials:

Search ClinicalTrials for Snca-Related Parkinson Disease

Search NIH Clinical Center for Snca-Related Parkinson Disease

Genetic Tests for Snca-Related Parkinson Disease

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Genetic tests related to Snca-Related Parkinson Disease:

id Genetic test Affiliating Genes
1 Snca-Related Parkinson Disease20 SNCA

Anatomical Context for Snca-Related Parkinson Disease

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Animal Models for Snca-Related Parkinson Disease or affiliated genes

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Publications for Snca-Related Parkinson Disease

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Variations for Snca-Related Parkinson Disease

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Expression for genes affiliated with Snca-Related Parkinson Disease

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Expression patterns in normal tissues for genes affiliated with Snca-Related Parkinson Disease

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

Pathways for genes affiliated with Snca-Related Parkinson Disease

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Compounds for genes affiliated with Snca-Related Parkinson Disease

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GO Terms for genes affiliated with Snca-Related Parkinson Disease

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Products for genes affiliated with Snca-Related Parkinson Disease

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  • Antibodies
  • Proteins
  • Lysates

Sources for Snca-Related Parkinson Disease

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3CDC
13ExPASy
14FMA
22GTR
23HGMD
24HMDB
25ICD10
26ICD10 via Orphanet
27ICD9CM
28IUPHAR
29KEGG
34MeSH
35MESH via Orphanet
36MGI
39NCIt
40NDF-RT
43NINDS
44Novoseek
46OMIM
47OMIM via Orphanet
51PubMed
52QIAGEN
58SNOMED-CT via Orphanet
62UMLS
63UMLS via Orphanet