Tay-Sachs disease AB variant (Q5513688)
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extremely rare, severe genetic disorder characterized by progressive neurological decline due to ganglioside activator deficiency
- Tay-Sachs disease, variant AB (disorder)
- Tay-Sachs disease, variant AB
- GM2-gangliosidosis, AB variant
- GM2-gangliosidosis variant AB
- Hexosaminidase activator deficiency
- GM2 gangliosidosis, AB variant
- Ab Variant Gm2-Gangliosidosis
- Gm2 Activator Deficiency
- Tay-Sachs Disease, Ab Variant
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Tay-Sachs disease AB variant |
extremely rare, severe genetic disorder characterized by progressive neurological decline due to ganglioside activator deficiency |
|
Statements
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Identifiers
Tay-Sachs Disease, AB Variant
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Sitelinks
Wikipedia(5 entries)
- bswiki AB varijanta GM2-gangliozidoze
- enwiki GM2-gangliosidosis, AB variant
- fiwiki Tyypin AB GM2-gangliosidoosi
- ruwiki GM2-ганглиозидоз (вариант АБ)
- srwiki АБ варијанта ГМ2 ганглиозидозе