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| Structural eye disease v0.76 | NYX | Nicola Ragge reviewed gene: NYX: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Night blindness, congenital stationary (complete), 1A, X-linked, 310500; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | NYX | Ivone Leong edited their review of gene: NYX: Changed phenotypes: Night blindness, congenital stationary (complete), 1A, X-linked, 310500 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | NYX | Ivone Leong reviewed gene: NYX: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Gyrate atrophy of choroid and retina with or without ornithinemia, 258870; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | NYX |
Ivone Leong Source NHS GMS was added to NYX. Mode of inheritance for gene NYX was changed from to X-LINKED: hemizygous mutation in males, biallelic mutations in females Added phenotypes Night blindness, congenital stationary (complete), 1A, X-linked, 310500 for gene: NYX |
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| Structural eye disease v0.2 | NYX |
Ellen McDonagh gene: NYX was added gene: NYX was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: NYX was set to Phenotypes for gene: NYX were set to Eye Disorders |
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