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Early onset dementia (encompassing fronto-temporal dementia and prion disease) v1.83 | ITM2B | Sarah Leigh Phenotypes for gene: ITM2B were changed from Dementia, familial British, 176500 to Dementia, familial British, OMIM:176500; ABri amyloidosis, MONDO:0008306; Dementia, familial Danish, OMIM:117300; ADan amyloidosis, MONDO:0007297 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Early onset dementia (encompassing fronto-temporal dementia and prion disease) v1.82 | ITM2B | Sarah Leigh Publications for gene: ITM2B were set to 10391242; 10781099 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Early onset dementia (encompassing fronto-temporal dementia and prion disease) v1.81 | ITM2B | Sarah Leigh Publications for gene: ITM2B were set to |