- OMIM ID
-
268800
- OMIM term:
- SANDHOFF DISEASE
- Alternative terms:
-
GM2-GANGLIOSIDOSIS, TYPE II
HEXOSAMINIDASES A AND B DEFICIENCY SANDHOFF DISEASE, ADULT TYPE, INCLUDED
SANDHOFF DISEASE, JUVENILE TYPE, INCLUDED
SANDHOFF DISEASE, INFANTILE TYPE, INCLUDED
- (∗) Location:
- 5q13.3
- (†) Associated OMIM genes:
- HEXB ENC1, ANTISENSE, INCLUDED; ENC1AS, INCLUDED
- (‡) Associated MGI genes:
- Hexb
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