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Primary immunodeficiency or monogenic inflammatory bowel disease v2.34 | SNX10 |
Louise Daugherty Source IUIS Classification December 2019 was added to SNX10. Mode of inheritance for gene SNX10 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Osteopetrosis with visual impairment; Defects in intrinsic and innate immunity for gene: SNX10 Publications for gene SNX10 were updated from to 32048120; 32086639 |
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Primary immunodeficiency or monogenic inflammatory bowel disease | SNX10 | Louise Daugherty commented on gene: SNX10 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Primary immunodeficiency or monogenic inflammatory bowel disease | SNX10 | Louise Daugherty reviewed gene: SNX10 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Primary immunodeficiency or monogenic inflammatory bowel disease | SNX10 | Louise Daugherty Added gene to panel |