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| Auditory Neuropathy v0.16 | PCDH9 | Bryony Thompson Marked gene: PCDH9 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Auditory Neuropathy v0.16 | PCDH9 | Bryony Thompson Gene: pcdh9 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Auditory Neuropathy v0.16 | PCDH9 | Bryony Thompson reviewed gene: PCDH9: Rating: RED; Mode of pathogenicity: None; Publications: 19353688; Phenotypes: Autosomal dominant auditory neuropathy 1; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Auditory Neuropathy v0.0 | PCDH9 |
Bryony Thompson gene: PCDH9 was added gene: PCDH9 was added to Auditory Neuropathy. Sources: Literature Mode of inheritance for gene: PCDH9 was set to Unknown Publications for gene: PCDH9 were set to 21176974 Phenotypes for gene: PCDH9 were set to Non-syndromic auditory neuropathy spectrum disorder |
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