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| Structural eye disease v0.76 | ARL13B | Nicola Ragge reviewed gene: ARL13B: Rating: RED; Mode of pathogenicity: ; Publications: 18674751, 25138100; Phenotypes: Joubert syndrome 8, 612291; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | ARL13B | Ivone Leong reviewed gene: ARL13B: Rating: RED; Mode of pathogenicity: ; Publications: 18674751, 25138100; Phenotypes: Joubert syndrome 8 612291; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.25 | ARL13B | Ivone Leong Phenotypes for gene: ARL13B were changed from Joubert syndrome 8 612291; Joubert syndrome 8 to Joubert syndrome 8 612291 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | ARL13B |
Ivone Leong Source NHS GMS was added to ARL13B. Added phenotypes Joubert syndrome 8 612291 for gene: ARL13B Publications for gene ARL13B were changed from 18674751; 25138100 to 25138100; 18674751 |
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| Structural eye disease v0.2 | ARL13B |
Ellen McDonagh gene: ARL13B was added gene: ARL13B was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: ARL13B was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: ARL13B were set to 18674751; 25138100 Phenotypes for gene: ARL13B were set to Joubert syndrome 8 |
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