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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 | ||||
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(HPO:0000505) | Visual impairment | rare [HPO:skoehler] | 297 / 7739 | |||
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(HPO:0000594) | Shallow anterior chamber | rare [HPO:skoehler] | 8 / 7739 | |||
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(HPO:0001146) | Pigmentary retinal degeneration | 15 / 7739 | ||||
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(HPO:0007663) | Reduced visual acuity | rare [HPO:skoehler] | 100 / 7739 | |||
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(HPO:0007917) | Tractional retinal detachment | rare [HPO:skoehler] | 2 / 7739 | |||
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(HPO:0030490) | Exudative vitreoretinopathy | 5 / 7739 |