MCID: LMB027
MIFTS: 16

Limb-Girdle Muscular Dystrophies, Autosomal Dominant malady

Muscle diseases category

Summaries for Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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MalaCards: Limb-Girdle Muscular Dystrophies, Autosomal Dominant is related to limb-girdle muscular dystrophy and myopathy. An important gene associated with Limb-Girdle Muscular Dystrophies, Autosomal Dominant is MYOT (myotilin). The compound creatinine have been mentioned in the context of this disorder.

Aliases & Classifications for Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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20GeneTests, 22GTR
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Classifications:

Malacards categories (disease lists): (See all malacards categories)
Anatomical: Muscle diseases


Aliases & Descriptions:

limb-girdle muscular dystrophies, autosomal dominant 20 22


Related Diseases for Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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17GeneCards, 18GeneDecks
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Graphical network of diseases related to Limb-Girdle Muscular Dystrophies, Autosomal Dominant:



Diseases related to limb-girdle muscular dystrophies, autosomal dominant

Clinical Features for Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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Drugs & Therapeutics for Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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5CenterWatch, 41NIH Clinical Center, 6ClinicalTrials
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Approved drugs:

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Drug clinical trials:

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Search NIH Clinical Center for Limb-Girdle Muscular Dystrophies, Autosomal Dominant

Search CenterWatch for Limb-Girdle Muscular Dystrophies, Autosomal Dominant

Genetic Tests for Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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20GeneTests, 22GTR
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Genetic tests related to Limb-Girdle Muscular Dystrophies, Autosomal Dominant:

id Genetic test Affiliating Genes
1 Limb-Girdle Muscular Dystrophies, Autosomal Dominant20 22 MYOT

Anatomical Context for Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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Animal Models for Limb-Girdle Muscular Dystrophies, Autosomal Dominant or affiliated genes

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Publications for Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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Genetic Variations for Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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Expression for genes affiliated with Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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1BioGPS, 15Gene Expression Omnibus DataSets
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Expression patterns in normal tissues for genes affiliated with Limb-Girdle Muscular Dystrophies, Autosomal Dominant

Search GEO for disease gene expression data for Limb-Girdle Muscular Dystrophies, Autosomal Dominant.

Pathways for genes affiliated with Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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Compounds for genes affiliated with Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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44Novoseek
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Compounds related to Limb-Girdle Muscular Dystrophies, Autosomal Dominant according to GeneCards/GeneDecks:

idCompoundScoreTop Affiliating Genes
1creatinine449.1LMNA, CAV3

GO Terms for genes affiliated with Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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16Gene Ontology
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Cellular components related to Limb-Girdle Muscular Dystrophies, Autosomal Dominant according to GeneCards/GeneDecks:

idNameGO IDScoreTop Affiliating Genes
1Z discGO:0300189.0MYOT, CAV3
2sarcolemmaGO:0423838.7MYOT, CAV3

Biological processes related to Limb-Girdle Muscular Dystrophies, Autosomal Dominant according to GeneCards/GeneDecks:

idNameGO IDScoreTop Affiliating Genes
1muscle organ developmentGO:0075179.1LMNA, CAV3

Products for genes affiliated with Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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  • Antibodies
  • Proteins
  • Lysates
  • Antibodies

Sources for Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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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
50PubMed
51QIAGEN
57SNOMED-CT via Orphanet
60UMLS
61UMLS via Orphanet