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(HPO:0000510) | Rod-cone dystrophy | 266 / 7739 | ||||
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(HPO:0000546) | Retinal degeneration | 61 / 7739 | ||||
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(HPO:0000662) | Nyctalopia | 92 / 7739 | ||||
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(HPO:0001133) | Constriction of peripheral visual field | 33 / 7739 | ||||
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(OMIM) | Retinitis pigmentosa type I(D) | 1 / 7739 | ||||
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(OMIM) | Midequatorial fundus pigmentation | 1 / 7739 | ||||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 | ||||
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(HPO:0007894) | Hypopigmentation of the fundus | 14 / 7739 | ||||
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(HPO:0011505) | Cystoid macular edema | rare [HPO:skoehler] | 8 / 7739 |