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| Structural eye disease v0.76 | SNRNP200 | Nicola Ragge reviewed gene: SNRNP200: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 33, 610359; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | SNRNP200 | Ivone Leong edited their review of gene: SNRNP200: Changed phenotypes: Retinitis pigmentosa 33, 610359 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | SNRNP200 | Ivone Leong reviewed gene: SNRNP200: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Leber congenital amaurosis 3, 604232, Retinitis pigmentosa, juvenile, autosomal recessive, 604232; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | SNRNP200 |
Ivone Leong Source NHS GMS was added to SNRNP200. Mode of inheritance for gene SNRNP200 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Retinitis pigmentosa 33, 610359 for gene: SNRNP200 |
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| Structural eye disease v0.2 | SNRNP200 |
Ellen McDonagh gene: SNRNP200 was added gene: SNRNP200 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: SNRNP200 was set to Phenotypes for gene: SNRNP200 were set to Eye Disorders |
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