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Tay-Sachs disease (Q560337)

From Wikidata
Human medical condition
  • hexosaminidase A deficiency
  • Tay-Sachs disease (disorder)
  • disease, Tay-Sachs
  • GM2 gangliosidosis, type 1
  • Hexosaminidase a Deficiency, Adult Type
  • Hexosaminidase alpha-subunit deficiency (variant B)
  • Gm2-Gangliosidosis, Variant B1
  • Gm2-Gangliosidosis, Adult Chronic Type
  • B variant GM2 gangliosidosis
  • Gm2-Gangliosidosis, Type 1
  • Hexa Deficiency
  • GM2 gangliosidosis, B, B1 variant
  • Sphingolipidosis, Tay-Sachs
  • TAY-SACHS DISEASE; TSD
  • TSD
  • Tay-Sachs Disease, Variant B1
  • Tay-Sachs Disease, Juvenile
  • Tay-Sachs Disease, Pseudo-Ab Variant
  • B Variant Gm2-Gangliosidosis
  • TAY-SACHS DISEASE
  • Gangliosidosis GM2 , type 1
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    English
    Tay-Sachs disease
    Human medical condition
    • hexosaminidase A deficiency
    • Tay-Sachs disease (disorder)
    • disease, Tay-Sachs
    • GM2 gangliosidosis, type 1
    • Hexosaminidase a Deficiency, Adult Type
    • Hexosaminidase alpha-subunit deficiency (variant B)
    • Gm2-Gangliosidosis, Variant B1
    • Gm2-Gangliosidosis, Adult Chronic Type
    • B variant GM2 gangliosidosis
    • Gm2-Gangliosidosis, Type 1
    • Hexa Deficiency
    • GM2 gangliosidosis, B, B1 variant
    • Sphingolipidosis, Tay-Sachs
    • TAY-SACHS DISEASE; TSD
    • TSD
    • Tay-Sachs Disease, Variant B1
    • Tay-Sachs Disease, Juvenile
    • Tay-Sachs Disease, Pseudo-Ab Variant
    • B Variant Gm2-Gangliosidosis
    • TAY-SACHS DISEASE
    • Gangliosidosis GM2 , type 1

    Statements

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    Tay-Sachs disease is an autosomal recessive, progressive neurodegenerative disorder (English)

    Identifiers

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    Tay-Sachs disease
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