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(HPO:0007641) | Dyschromatopsia | 19 / 7739 | ||||
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(HPO:0007754) | Macular dystrophy | 26 / 7739 | ||||
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(HPO:0008001) | Foveal hyperpigmentation | 2 / 7739 | ||||
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(OMIM) | Normal findings on electrophysiologic testing | 1 / 7739 | ||||
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(OMIM) | Benign concentric annular macular dystrophy | 1 / 7739 | ||||
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(OMIM) | Depigmented ring around an intact central area | 1 / 7739 | ||||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |