(Q560337)

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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MONDO:0010100
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Tay-Sachs disease
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