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| Night blindness, congenital stationary (complete), 1C, autosomal recessive, 613216 (3): Located in omimdefinitions
| * 605837 HECT DOMAIN AND RCC1-LIKE DOMAIN 2| HERC2: Located in omimdefinitions
| [Skin/hair/eye pigmentation 1, blond/brown hair], 227220 (3): Located in omimdefinitions
| Mental retardation, autosomal recessive 38, 615516 (3): Located in omimdefinitions
| Ciliary dyskinesia, primary, 4 (2): Located in omimdefinitions
| Legius syndrome, 611431 (3): Located in omimdefinitions
| Interstitial nephritis, karyomegalic, 614817 (3): Located in omimdefinitions
| Chromosome 15q13.3 microdeletion syndrome (4): Located in omimdefinitions
| * 606934 NADH DEHYDROGENASE (UBIQUINONE) COMPLEX I, ASSEMBLY FACTOR 1| NDUFAF1: Located in omimdefinitions
| Cardiomyopathy, dilated, 1R, 613424 (3): Located in omimdefinitions

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