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- Q55787389 description "#946;2M) leading to progressive gastrointestinal dysfunction, SjC6gren syndrome (see this term) and autonomic neuropathy" @default.
- Q55787389 name "variant ABeta2M amyloidosis" @default.
- Q55787389 type Item @default.
- Q55787389 label "variant ABeta2M amyloidosis" @default.
- Q55787389 altLabel "Autosomal dominant beta2-microglobulinic amyloidosis" @default.
- Q55787389 prefLabel "variant ABeta2M amyloidosis" @default.
- Q55787389 P1550 Q55787389-B16F86A9-B0E2-4E18-A92C-A72C8FE3FA28 @default.
- Q55787389 P279 Q55787389-5483A63B-E517-463F-8C25-9C796B569ADE @default.
- Q55787389 P279 Q55787389-7BFC9A54-2280-4438-BE54-9F48BD64B1BC @default.
- Q55787389 P2888 Q55787389-1043C3C7-B750-4082-A48A-4E6824B58792 @default.
- Q55787389 P31 Q55787389-D9322D51-0B8E-4930-BABF-2F73E2DDA48A @default.
- Q55787389 P4229 Q55787389-983ABC0B-748D-4C5E-B907-D0DD99E9F5BB @default.
- Q55787389 P5270 Q55787389-6B407E71-928C-436F-96B8-1AAAEE26F86B @default.
- Q55787389 P5270 MONDO_0017810 @default.
- Q55787389 P1550 "314652" @default.
- Q55787389 P279 Q55788199 @default.
- Q55787389 P279 Q5737919 @default.
- Q55787389 P2888 Orphanet_314652 @default.
- Q55787389 P31 Q112193867 @default.
- Q55787389 P4229 "E85.1" @default.
- Q55787389 P5270 "MONDO_0017810" @default.