- ... Description GM2 activator deficiency (sometimes called GM2 gangliosidosis, AB variant) is a rare inherited disorder that causes progressive ... condition. Other Names for This Condition GM2 gangliosidosis, AB variant Hexosaminidase activator deficiency Tay-Sachs disease, AB variant ...
- ... p >GM2 activator deficiency (sometimes called GM2 gangliosidosis, AB variant) is a rare inherited disorder that causes progressive ... related-gene-list><synonym-list ><synonym >GM2 gangliosidosis, AB variant</synonym><synonym >Hexosaminidase activator deficiency</synonym><synonym >Tay- ...
- ... deficiency</title><other_names ><other_name >GM2 gangliosidosis, AB variant</other_name><other_name >Hexosaminidase activator deficiency</other_ ...
- ... with GM2 activator deficiency (sometimes called GM2 gangliosidosis, AB variant). This is a rare inherited disorder that results ... activator deficiency in two patients with GM2-gangliosidosis AB variant. Am J Hum Genet. 1996 Nov;59(5): ...
- Neurodegenerative (degenerative nerve) diseases are disorders that destroy motor neurons. Parkinson's is an examples. See a list of all the diseases. ... Degenerative nerve ...
- ... hypomyelination on T 2 -weighted images GM2-gangliosidosis, AB variant AR GM2A Indistinguishable from GM1-gangliosidosis Leukodystrophies Creatine ...
- ... Aspartylglucosaminuria GM1 gangliosidosis GM2 activator deficiency GM2 gangliosidosis, AB variant, see GM2 activator deficiency GM2 gangliosidosis, type 1, ...
- Tay-Sachs disease is a rare genetic disorder. It causes too much of a fatty substance to build up in the brain, which destroys nerve cells. ... Tay-Sachs disease ...
- ... overgrowth syndrome Tay-Sachs disease Tay-Sachs disease, AB variant, see GM2 activator deficiency Taybi syndrome, see Otopalatodigital ...
- ... are called Tay-Sachs disease and GM2-gangliosidosis, AB variant , which are caused by variants in other genes. ...
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