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| Mendeliome v2.8 | PDE1C | Sangavi Sivagnanasundram reviewed gene: PDE1C: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v2.0 | PDE1C | Gene migrated from ENSG00000154678 to ENSG00000154678 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v1.4379 | PDE1C |
Bryony Thompson gene: PDE1C was added gene: PDE1C was added to Mendeliome. 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 Review for gene: PDE1C was set to RED Added comment: A single family reported. Sources: Literature |
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