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| Structural eye disease v0.76 | BBS5 | Nicola Ragge reviewed gene: BBS5: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Bardet-Biedl syndrome5, 615983; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | BBS5 | Ivone Leong reviewed gene: BBS5: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Bardet-Biedl syndrome5, 615983; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | BBS5 |
Ivone Leong Source NHS GMS was added to BBS5. Mode of inheritance for gene BBS5 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Bardet-Biedl syndrome5, 615983 for gene: BBS5 |
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| Structural eye disease v0.2 | BBS5 |
Ellen McDonagh gene: BBS5 was added gene: BBS5 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: BBS5 was set to Phenotypes for gene: BBS5 were set to Eye Disorders |
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