Muscular Dystrophy, Limb-Girdle, Type 1h (LGMD1H)

Alias:
Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1h
Lgmd1h
Dystrophy, Muscular, Limb-Girdle, Type 1h
Muscular Dystrophy Limb-Girdle Type 1h
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Muscular Dystrophy, Limb-Girdle, Type 1h, also known as autosomal dominant limb-girdle muscular dystrophy type 1h, is related to limb-girdle muscular dystrophy and muscular dystrophy. An important gene associated with Muscular Dystrophy, Limb-Girdle, Type 1h is LGMD1H (Limb Girdle Muscular Dystrophy 1H (Autosomal Dominant)). Affiliated tissues include skeletal muscle, and related phenotypes are centrally nucleated skeletal muscle fibers and muscle weakness

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Adolescent
--
7
33
1

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Mutations
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Related Drugs

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Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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