Muscular Dystrophy-Dystroglycanopathy , Type a, 11 (MDDGA11)

Alias:
Mddga11
Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies, Type a, 11
Muscular Dystrophy-Dystroglycanopathy Congenital with Brain and Eye Anomalies A11
Walker-Warburg Syndrome or Muscle-Eye-Brain Disease, B3galnt2-Related
Walker-Warburg Syndrome or Muscle-Eye-Brain Disease B3galnt2-Related
Dystrophy, Muscular, Dystroglycanopathy , Type A11
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Muscular Dystrophy-Dystroglycanopathy , Type a, 11, also known as mddga11, is related to congenital muscular dystrophy-dystroglycanopathy type a11. An important gene associated with Muscular Dystrophy-Dystroglycanopathy , Type a, 11 is B3GALNT2 (Beta-1,3-N-Acetylgalactosaminyltransferase 2). Affiliated tissues include eye and brain.
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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2
10
12

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
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No data available

Gene & Mutation

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Related Drugs

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No data available

Disease Model

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

References Literature

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