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| * 179095 UBIQUITIN-CONJUGATING ENZYME E2B| UBE2B: Located in omimdefinitions
| {Schizophrenia}, 181500 (2): Located in omimdefinitions
| D-bifunctional protein deficiency, 261515 (3): Located in omimdefinitions
| Perrault syndrome 1, 233400 (3): Located in omimdefinitions
| Leukodystrophy, adult-onset, autosomal dominant, 169500 (3): Located in omimdefinitions
| Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, 614399 (3): Located in omimdefinitions
| * 612453 MULTIPLE EPIDERMAL GROWTH FACTOR-LIKE DOMAINS 10| MEGF10: Located in omimdefinitions
| ?Mitochondrial complex III deficiency, nuclear type 8, 615838 (3): Located in omimdefinitions
| * 604443 ACYL-CoA SYNTHETASE LONG CHAIN FAMILY, MEMBER 6| ACSL6: Located in omimdefinitions
| Myelogenous leukemia, acute (3): Located in omimdefinitions

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