(Q917227)
English
Sandhoff disease
lysosomal storage disorder from the GM2 gangliosidosis family, characterised by central nervous system degeneration
- Sandhoff disease (disorder)
- Sandhoff Jatzkewitz disease
- Sandhoff Disease, Juvenile Type
- Hexosaminidases a and B Deficiency
- Gm2-Gangliosidosis, Type 2
- GM2 gangliosidosis 0 variant
- SANDHOFF DISEASE
- Sandhoff Disease, Adult Type
- Sandhoff Disease, Infantile Type
Statements
2 references
1 reference
3 references
1 reference
Identifiers
Sandhoff Disease
1 reference
1 reference
2 references
1 reference
1 reference
Sitelinks
Wikipedia(12 entries)
- arwiki داء ساندهوف
- bswiki Sandhoffova bolest
- dewiki Sandhoff-Krankheit
- enwiki Sandhoff disease
- eswiki Enfermedad de Sandhoff
- euwiki Sandhoffen gaixotasun
- fawiki بیماری سندهوف
- fiwiki Sandhoffin tauti
- ptwiki Doença de Sandhoff
- ruwiki Синдром Сандхоффа
- srwiki Сандхофова болест
- ttwiki Сандхофф чире