Tay-Sachs Disease, B Variant, Infantile Form

Alias:

Gm2 Gangliosidosis, B Variant, Infantile Form

Hexosaminidase a Deficiency, Infantile Form

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Basic Information

Medical Symptom

Gene & Mutation

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Disease Model

References Literature

Tay-Sachs Disease, B Variant, Infantile Form, is also known as gm2 gangliosidosis, b variant, infantile form. An important gene associated with Tay-Sachs Disease, B Variant, Infantile Form is HEXA (Hexosaminidase Subunit Alpha). Affiliated tissues include eye.

Related ID：

MALACARDS：TYS004