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Structural eye disease v0.76 | TRIM32 | Nicola Ragge reviewed gene: TRIM32: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Bardet-Biedl syndrome 11, Muscular dystrophy, limb-girdle, type 2H, 615988, 254110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.48 | TRIM32 | Ivone Leong edited their review of gene: TRIM32: Changed phenotypes: Bardet-Biedl syndrome 11, 615988, Muscular dystrophy, limb-girdle, type 2H, 254110 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.38 | TRIM32 | Ivone Leong reviewed gene: TRIM32: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ANIRIDIA 3, 617142; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.15 | TRIM32 |
Ivone Leong Source NHS GMS was added to TRIM32. Mode of inheritance for gene TRIM32 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Bardet-Biedl syndrome 11, 615988; Muscular dystrophy, limb-girdle, type 2H, 254110 for gene: TRIM32 |
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Structural eye disease v0.2 | TRIM32 |
Ellen McDonagh gene: TRIM32 was added gene: TRIM32 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: TRIM32 was set to Phenotypes for gene: TRIM32 were set to Eye Disorders |