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The way concept relations are shown:
Sandhoff Disease
Hierarchy: | ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease 4 coordinate conceptsX |
Broader terms: | ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sandhoff Disease |
History note: | G(M2) Ganglioside (1975-1978) | Gangliosides (1966-1978) | Gangliosidosis (1976-1978) | Hexosaminidases (1971-1978) | Lipoidosis (1966-1978) | Sphingolipidosis (1974-1978)X |
historyNote*: | 1979
X |
publicMeSHNote*: | 1979
X |
Scope note: | An autosomal recessive neurodegenerative disorder characterized by an accumulation of G(M2) GANGLIOSIDE in neurons and other tissues. It is caused by mutation in the common beta subunit of HEXOSAMINIDASE A and HEXOSAMINIDASE B. Thus this disease is also known as the O variant since both hexosaminidase A and B are missing. Clinically, it is indistinguishable from TAY-SACHS DISEASE.
X |
activeMeSHYear*: | 2007X |
dateCreated*: | 1978-05-22X |
dateEstablished*: | 1979-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | RCX |
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Labels and equivalent concepts: | Sandhoffin tauti (fi) XSandhoffs sjukdom (sv) Sandhoff Disease, Infantile (en, replaced) Sandhoff Disease, Juvenile (en, replaced) Sandhoff's Disease (en, replaced) Sandhoff Disease, Adult (en, replaced) Hexosaminidase A and B Deficiency Disease (en, replaced) G(M2) Gangliosidosis, Type II (en, replaced) Gangliosidosis G(M2), Type II (en, replaced) Gangliosidosis GM2, Type II (en, replaced) GM2 Gangliosidosis, Type II (en, replaced) Deficiency Disease, Hexosaminidase A and B (en, replaced) Morbus Sandhoff (la-FI, replaced) |
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