All diseases

OMIM ID
272750
OMIM term:
GM2-GANGLIOSIDOSIS, AB VARIANT
Alternative terms:
HEXOSAMINIDASE ACTIVATOR DEFICIENCY
GM2 ACTIVATOR DEFICIENCY
AB VARIANT GM2-GANGLIOSIDOSIS
TAY-SACHS DISEASE, AB VARIANT
(∗) Location:
5q33.1  
(†) Associated OMIM genes:
GM2A  
(‡) Associated MGI genes:
Gm2a  

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