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| Deafness_IsolatedAndComplex v2.0 | PDE1C | Gene migrated from ENSG00000154678 to ENSG00000154678 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v1.328 | Bryony Thompson Copied gene PDE1C from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v1.328 | PDE1C |
Bryony Thompson gene: PDE1C was added gene: PDE1C was added to Deafness_IsolatedAndComplex. Sources: Literature Mode of inheritance for gene: PDE1C was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: PDE1C were set to 29860631 Phenotypes for gene: PDE1C were set to autosomal dominant nonsyndromic hearing loss MONDO:0019587 |
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