All diseases

OMIM ID
272800
OMIM term:
TAY-SACHS DISEASE; TSD
Alternative terms:
GM2-GANGLIOSIDOSIS, TYPE I
B VARIANT GM2-GANGLIOSIDOSIS
HEXOSAMINIDASE A DEFICIENCY
HEXA DEFICIENCY TAY-SACHS DISEASE, JUVENILE, INCLUDED
HEXOSAMINIDASE A DEFICIENCY, ADULT TYPE, INCLUDED
GM2-GANGLIOSIDOSIS, ADULT CHRONIC TYPE, INCLUDED
GM2-GANGLIOSIDOSIS, VARIANT B1, INCLUDED
TAY-SACHS DISEASE, VARIANT B1, INCLUDED
TAY-SACHS DISEASE, PSEUDO-AB VARIANT, INCLUDED
(∗) Location:
15q23  
(†) Associated OMIM genes:
HEXA  
(‡) Associated MGI genes:
Hexa  

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