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| Structural eye disease v0.76 | PRCD | Nicola Ragge reviewed gene: PRCD: Rating: RED; Mode of pathogenicity: Other - please provide details in the comments; Publications: ; Phenotypes: Retinitis pigmentosa 36, 610599; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | PRCD | Ivone Leong edited their review of gene: PRCD: Changed phenotypes: Retinitis pigmentosa 36, 610599 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | PRCD | Ivone Leong reviewed gene: PRCD: Rating: RED; Mode of pathogenicity: Other - please provide details in the comments; Publications: ; Phenotypes: Stargardt disease 4, 603786, Macular dystrophy, retinal, 2, 608051, Retinitis pigmentosa 41, 612095, Cone-rod dystrophy 12, 612657; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | PRCD |
Ivone Leong Source NHS GMS was added to PRCD. Mode of inheritance for gene PRCD was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Retinitis pigmentosa 36, 610599 for gene: PRCD |
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| Structural eye disease v0.2 | PRCD |
Ellen McDonagh gene: PRCD was added gene: PRCD was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: PRCD was set to Phenotypes for gene: PRCD were set to Eye Disorders |
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