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| Atrial fibrillation, familial, 8 (2): Located in omimdefinitions
| Chromosome 16q22 deletion syndrome (4): Located in omimdefinitions
| * 121360 CORE-BINDING FACTOR, BETA SUBUNIT| CBFB: Located in omimdefinitions
| Macular corneal dystrophy, 217800 (3): Located in omimdefinitions
| Cirrhosis, North American Indian childhood type, 604901 (3): Located in omimdefinitions
| Miller syndrome, 263750 (3): Located in omimdefinitions
| Apparent mineralocorticoid excess, 218030 (3): Located in omimdefinitions
| Mitochondrial DNA depletion syndrome 2 (myopathic type), 609560 (3): Located in omimdefinitions
| Cataract, pulverulent or cerulean, with or without microcornea, 610202 (3): Located in omimdefinitions
| * 192090 CADHERIN 1| CDH1: Located in omimdefinitions

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