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| Structural eye disease v0.76 | WHRN | Nicola Ragge reviewed gene: WHRN: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Usher syndrome, type 2D, 611383; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | WHRN | Ivone Leong edited their review of gene: WHRN: Changed phenotypes: Usher syndrome, type 2D, 611383 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | WHRN | Ivone Leong reviewed gene: WHRN: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: WILMS TUMOR,ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATION SYNDROME, 194072; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | WHRN |
Ivone Leong Source NHS GMS was added to WHRN. Mode of inheritance for gene WHRN was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Usher syndrome, type 2D, 611383 for gene: WHRN |
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| Structural eye disease v0.2 | WHRN |
Ellen McDonagh gene: WHRN was added gene: WHRN was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: WHRN was set to Phenotypes for gene: WHRN were set to Eye Disorders |
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