- OMIM ID
-
598500
- OMIM term:
- WOLFRAM SYNDROME, MITOCHONDRIAL FORM
- Alternative terms:
-
DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS, MITOCHONDRIAL FORM
DIDMOAD SYNDROME, MITOCHONDRIAL FORM
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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