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The way concept relations are shown:
Tay-Sachs Disease
Hierarchy: | ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease 2 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease 2 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease 2 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease 2 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease 2 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease 2 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease 2 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease 2 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease 2 coordinate conceptsX |
Broader terms: | ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Tay-Sachs Disease |
Annotation: | TAY-SACHS DISEASE, AB VARIANT is also available
X |
History note: | Lipoidosis (1966-1978)X |
historyNote*: | 1979; for AMAUROTIC FAMILIAL IDIOCY use LIPOIDOSIS 1985-2006
X |
publicMeSHNote*: | 1979; see AMAUROTIC FAMILIAL IDIOCY 1963-1978; for AMAUROTIC FAMILIAL IDIOCY see LIPOIDOSIS 1985-2006, see AMAUROTIC FAMILIAL IDIOCY 1963-1978
X |
Scope note: | An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry.
X |
activeMeSHYear*: | 2007X |
dateCreated*: | 1978-05-22X |
dateEstablished*: | 1979-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | RCX |
Related term: | |
Type: | |
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Labels and equivalent concepts: | Tay-Sachsin tauti (fi) XHexosaminidase A Deficiency Disease (en, replaced) GM2 Gangliosidosis, Type I (en, replaced) GM2 Gangliosidosis, B Variant (en, replaced) Gangliosidosis GM2, Type I (en, replaced) Tay-Sachs Disease, B Variant (en, replaced) Gangliosidosis GM2, B Variant (en, replaced) Gangliosidosis G(M2), Type I (en, replaced) G(M2) Gangliosidosis, Type I (en, replaced) Familial Amaurotic Idiocy (en, replaced) Deficiency Disease Hexosaminidase A (en, replaced) Enfermedad de Tay-Sachs (es) νόσος Tay-Sachs (el) Tay-Sachs-Krankheit (de) Tayova-Sachsova nemoc (cs) Enfermedad de Tay-Sachs Variante B (es, replaced) Gangliosidosis GM2 Variante B (es, replaced) Gangliosidosis G(M2) Tipo I (es, replaced) Enfermedad por Deficiencia de Hexosaminidasa A (es, replaced) Gangliosidose-GM2, Typ I (de, replaced) Gangliosidose-G(M2), Typ I (de, replaced) G(M2)-Gangliosidose, Typ I (de, replaced) GM2-Gangliosidose, Typ I (de, replaced) Hexosaminidase-A-Mangelkrankheit (de, replaced) Amaurotische familiäre Idiotie (de, replaced) |
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