MCID: MSH005

Msh6-Related Lynch Syndrome malady

Genetic diseases, Cancer diseases, Rare diseases, Gastrointestinal diseases categories
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Summaries for Msh6-Related Lynch Syndrome

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MalaCards based summary: Msh6-Related Lynch Syndrome, is also known as hereditary nonpolyposis colorectal cancer An important gene associated with Msh6-Related Lynch Syndrome is MSH6 (mutS homolog 6).

Aliases & Classifications for Msh6-Related Lynch Syndrome

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Msh6-Related Lynch Syndrome, Aliases & Descriptions:

Name: Msh6-Related Lynch Syndrome 20
 
Hereditary Nonpolyposis Colorectal Cancer 62


Classifications:



Related Diseases for Msh6-Related Lynch Syndrome

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Symptoms for Msh6-Related Lynch Syndrome

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Drugs & Therapeutics for Msh6-Related Lynch Syndrome

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Drug clinical trials:

Search ClinicalTrials for Msh6-Related Lynch Syndrome

Search NIH Clinical Center for Msh6-Related Lynch Syndrome

Genetic Tests for Msh6-Related Lynch Syndrome

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Genetic tests related to Msh6-Related Lynch Syndrome:

id Genetic test Affiliating Genes
1 Msh6-Related Lynch Syndrome20 MSH6

Anatomical Context for Msh6-Related Lynch Syndrome

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Animal Models for Msh6-Related Lynch Syndrome or affiliated genes

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Publications for Msh6-Related Lynch Syndrome

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Variations for Msh6-Related Lynch Syndrome

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Expression for genes affiliated with Msh6-Related Lynch Syndrome

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Expression patterns in normal tissues for genes affiliated with Msh6-Related Lynch Syndrome

Search GEO for disease gene expression data for Msh6-Related Lynch Syndrome.

Pathways for genes affiliated with Msh6-Related Lynch Syndrome

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Compounds for genes affiliated with Msh6-Related Lynch Syndrome

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GO Terms for genes affiliated with Msh6-Related Lynch Syndrome

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Products for genes affiliated with Msh6-Related Lynch Syndrome

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  • Antibodies
  • Proteins
  • Lysates

Sources for Msh6-Related Lynch Syndrome

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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