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| Structural eye disease v0.76 | BBS9 | Nicola Ragge reviewed gene: BBS9: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Bardet-Biedl syndrome9, 615986; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | BBS9 | Ivone Leong reviewed gene: BBS9: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Bardet-Biedl syndrome9, 615986; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | BBS9 |
Ivone Leong Source NHS GMS was added to BBS9. Mode of inheritance for gene BBS9 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Bardet-Biedl syndrome9, 615986 for gene: BBS9 |
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| Structural eye disease v0.2 | BBS9 |
Ellen McDonagh gene: BBS9 was added gene: BBS9 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: BBS9 was set to Phenotypes for gene: BBS9 were set to Eye Disorders |
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