Matches in Wikidata for { <http://www.wikidata.org/entity/Q55786561> ?p ?o ?g. }
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- Q55786561 description "human disease" @default.
- Q55786561 description "хвороба людини" @default.
- Q55786561 name "Mowat-Wilson syndrome due to monosomy 2q22" @default.
- Q55786561 type Item @default.
- Q55786561 label "Mowat-Wilson syndrome due to monosomy 2q22" @default.
- Q55786561 altLabel "Hirschsprung disease and intellectual disability due to 2q22 microdeletion" @default.
- Q55786561 altLabel "Hirschsprung disease and intellectual disability due to del(2)(q22)" @default.
- Q55786561 altLabel "Hirschsprung disease and intellectual disability due to monosomy 2q22" @default.
- Q55786561 altLabel "Mowat-Wilson syndrome due to 2q22 microdeletion" @default.
- Q55786561 altLabel "Mowat-Wilson syndrome due to del(2)q(22)" @default.
- Q55786561 altLabel "Mowat-Wilson syndrome due to monosomy type 2q22" @default.
- Q55786561 prefLabel "Mowat-Wilson syndrome due to monosomy 2q22" @default.
- Q55786561 P1550 Q55786561-989C3C58-7426-4392-9A56-BAADCAEE4563 @default.
- Q55786561 P279 Q55786561-83730652-51E8-4BE5-B72E-B518E043F3ED @default.
- Q55786561 P279 Q55786561-FA5B3B59-6D95-4A95-B1EB-FD4486661D3C @default.
- Q55786561 P2888 Q55786561-CF19C65B-478D-4A8E-AB71-6AE284646AD4 @default.
- Q55786561 P31 Q55786561-A400DC3A-A7E6-4085-8AB2-6236CE32E019 @default.
- Q55786561 P31 Q55786561-E220023C-D9FE-4CAB-A1A7-103CFA52F6C9 @default.
- Q55786561 P4229 Q55786561-D73B7C3D-70E0-41CC-B1B4-AEFDACA08E56 @default.
- Q55786561 P5270 Q55786561-E2BDDFCA-BB3D-48D4-9118-019C7F715754 @default.
- Q55786561 P5270 MONDO_0016855 @default.
- Q55786561 P1550 "261537" @default.
- Q55786561 P279 Q2757585 @default.
- Q55786561 P279 Q39048665 @default.
- Q55786561 P2888 Orphanet_261537 @default.
- Q55786561 P31 Q112193867 @default.
- Q55786561 P31 Q55788864 @default.
- Q55786561 P4229 "Q43.1" @default.
- Q55786561 P5270 "MONDO_0016855" @default.