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(HPO:0007703) | Abnormality of retinal pigmentation | 21 / 7739 | ||||
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(HPO:0012508) | Metamorphopsia | 3 / 7739 | ||||
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(OMIM) | Grouped pigmentation of retinal fovea | 1 / 7739 | ||||
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(HPO:0000007) | Autosomal recessive inheritance | 2538 / 7739 |