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| Ataxia - paediatric v0.187 | BBS9 | Zornitza Stark Marked gene: BBS9 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia - paediatric v0.187 | BBS9 | Zornitza Stark Gene: bbs9 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia - paediatric v0.21 | BBS9 |
Bryony Thompson gene: BBS9 was added gene: BBS9 was added to Ataxia - paediatric_RMH. Sources: Expert list Mode of inheritance for gene: BBS9 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: BBS9 were set to Bardet-Biedl syndrome 9, 615986 Review for gene: BBS9 was set to RED Added comment: Ataxia is not a reported feature of the phenotype for this subtype of BBS. Sources: Expert list |
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