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(HPO:0000512) | Abnormal electroretinogram | Frequent [HPO:probinson] | 17924349 | IBIS | 61 / 7739 | |
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(HPO:0001123) | Visual field defect | Frequent [HPO:probinson] | 17924349 | IBIS | 30 / 7739 | |
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(HPO:0007843) | Attenuation of retinal blood vessels | 17924349 | IBIS | 25 / 7739 | ||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 | ||||
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(HPO:0000510) | Rod-cone dystrophy | 266 / 7739 | ||||
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(HPO:0007722) | Retinal pigment epithelial atrophy | 10 / 7739 |