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| Structural eye disease v0.76 | OAT | Nicola Ragge reviewed gene: OAT: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Gyrate atrophy of choroid and retina with or without ornithinemia, 258870; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | OAT | Ivone Leong edited their review of gene: OAT: Changed phenotypes: Gyrate atrophy of choroid and retina with or without ornithinemia, 258870 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | OAT | Ivone Leong reviewed gene: OAT: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Albinism, brown oculocutaneous, 203200, Albinism oculocutaneous, type II, [Skin/hair/eye pigmentation 1, blond/brown hair], 227220, [Skin/hair/eye pigmentation 1, blue/nonblue eyes]; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | OAT |
Ivone Leong Source NHS GMS was added to OAT. Mode of inheritance for gene OAT was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Gyrate atrophy of choroid and retina with or without ornithinemia, 258870 for gene: OAT |
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| Structural eye disease v0.2 | OAT |
Ellen McDonagh gene: OAT was added gene: OAT was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: OAT was set to Phenotypes for gene: OAT were set to Eye Disorders |
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