MCID: LMB027
MIFTS: 12

Limb-Girdle Muscular Dystrophies, Autosomal Dominant malady

Genetic diseases, Muscle diseases, Neuronal diseases, Rare diseases categories
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Summaries for Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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33MalaCards
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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).

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)
Global: Genetic diseases, Rare diseases
Anatomical: Muscle diseases, Neuronal 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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Diseases in the Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1h family:

limb-girdle muscular dystrophies, autosomal dominant Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1g
Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1e

Diseases related to Limb-Girdle Muscular Dystrophies, Autosomal Dominant via text searches within MalaCards or GeneCards/GeneDecks gene sharing:

idRelated DiseaseScoreTop Affiliating Genes
1limb-girdle muscular dystrophy10.4
2myopathy10.4

Symptoms for Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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

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42NIH Clinical Center, 6ClinicalTrials
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Drug clinical trials:

Search ClinicalTrials for Limb-Girdle Muscular Dystrophies, Autosomal Dominant

Search NIH Clinical Center 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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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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Sources:
2BioGPS, 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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GO Terms for genes affiliated with Limb-Girdle Muscular Dystrophies, Autosomal Dominant

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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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4CDC
13ExPASy
14FMA
22GTR
23HGMD
24HMDB
25ICD10
26ICD10 via Orphanet
27ICD9CM
29IUPHAR
30KEGG
35MeSH
36MESH via Orphanet
37MGI
40NCIt
41NDF-RT
44NINDS
45Novoseek
47OMIM
48OMIM via Orphanet
52PubMed
53QIAGEN
59SNOMED-CT via Orphanet
62UMLS
63UMLS via Orphanet