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| IBMDx study v0.38 | DIAPH1 |
Chirag Patel Source IBMDx Study was removed from DIAPH1. Mode of inheritance for gene DIAPH1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: DIAPH1 were changed from Macrothrombocytopenia and sensorineural hearing loss to DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome, MONDO:0044635 Publications for gene DIAPH1 were changed from 27707755, 27808407, 28003573, 28815995, 26912466 to 27707755, 27808407, 28003573, 28815995, 26912466 |
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| IBMDx study v0.0 | DIAPH1 |
Zornitza Stark gene: DIAPH1 was added gene: DIAPH1 was added to IBMDx study. Sources: IBMDx Study,Expert Review Green Mode of inheritance for gene: DIAPH1 was set to Unknown Phenotypes for gene: DIAPH1 were set to Macrothrombocytopenia and sensorineural hearing loss |
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