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| Carnitine deficiency, systemic primary, 212140 (3): Fundet i omimdefinitions
| Mitochondrial complex III deficiency, nuclear type 4, 615159 (3): Fundet i omimdefinitions
| Deafness, autosomal dominant 52 (2): Fundet i omimdefinitions
| Epilepsy, generalized, with febrile seizures plus, type 3, 611277 (3): Fundet i omimdefinitions
| {Epilepsy, childhood absence, susceptibility to, 2}, 607681 (3): Fundet i omimdefinitions
| * 137164 GAMMA-AMINOBUTYRIC ACID RECEPTOR, GAMMA-2| GABRG2: Fundet i omimdefinitions
| {Diabetes mellitus, insulin-dependent, 18} (2): Fundet i omimdefinitions
| * 161561 INTERLEUKIN 12B| IL12B: Fundet i omimdefinitions
| {Asthma, susceptibility to}, 600807 (3): Fundet i omimdefinitions
| {Psoriasis susceptibility 11} (2): Fundet i omimdefinitions

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