- OMIM ID
-
609241
- OMIM term:
- SCHINDLER DISEASE, TYPE I
- Alternative terms:
-
NEUROAXONAL DYSTROPHY, SCHINDLER TYPE
ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE I
NAGA DEFICIENCY, TYPE I ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE III, INCLUDED
NAGA DEFICIENCY, TYPE III, INCLUDED
SCHINDLER DISEASE, TYPE III, INCLUDED
- (∗) Location:
- 22q13.2
- (†) Associated OMIM genes:
- NAGA
- (‡) Associated MGI genes:
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