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ENTay-Sachs Disease, B Variant, Juvenile Form
Alias:
Gm2 Gangliosidosis, B Variant, Juvenile Form
Hexosaminidase a Deficiency, Juvenile Form
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Tay-Sachs Disease, B Variant, Juvenile Form, is also known as gm2 gangliosidosis, b variant, juvenile form. An important gene associated with Tay-Sachs Disease, B Variant, Juvenile Form is HEXA (Hexosaminidase Subunit Alpha). Affiliated tissues include eye.
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Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
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Score
Mutations
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Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
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References Literature
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IF
