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MIRAGE
GM2 gangliosidosis, AB variant
Summary
- Synonym
-
- GM2 Activator Deficiency
- Tay-Sachs disease AB variant
- Tay-Sachs disease, variant AB
- Definition
- A GM2 gangliosidosis that is characterized by normal hexosaminidase A (HEXA) and hexosaminidase B (HEXB) but the inability to form a functional GM2 activator complex.
- Super Class
- GM2 gangliosidosis
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P17900 | Ganglioside GM2 activator |
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q60648 | Ganglioside GM2 activator |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002421 | Poor head control |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000726 | Dementia |
| HP:0003593 | Infantile onset |
| HP:0001263 | Global developmental delay |
| HP:0008936 | Axial hypotonia |
| HP:0001285 | Spastic tetraparesis |
| HP:0003470 | Paralysis |
