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| Structural eye disease v0.76 | CEP41 | Nicola Ragge reviewed gene: CEP41: Rating: RED; Mode of pathogenicity: ; Publications: 22246503; Phenotypes: Joubert syndrome 15, 614464; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | CEP41 | Ivone Leong reviewed gene: CEP41: Rating: RED; Mode of pathogenicity: ; Publications: 22246503; Phenotypes: Joubert syndrome 15, 614464; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | CEP41 |
Ivone Leong Source NHS GMS was added to CEP41. Added phenotypes Joubert syndrome 15, 614464 for gene: CEP41 |
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| Structural eye disease v0.2 | CEP41 |
Ellen McDonagh gene: CEP41 was added gene: CEP41 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: CEP41 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: CEP41 were set to 22246503 Phenotypes for gene: CEP41 were set to Joubert syndrome |
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