Matches in Wikidata for { <http://www.wikidata.org/entity/Q55786361> ?p ?o ?g. }
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- Q55786361 description "8p23.1 deletion involves a partial deletion of the short arm of chromosome 8 characterized by low birth weight, postnatal growth deficiency, mild intellectual deficit, hyperactivity, craniofacial abnormalities, and congenital heart defects." @default.
- Q55786361 name "8p23.1 microdeletion syndrome" @default.
- Q55786361 type Item @default.
- Q55786361 label "8p23.1 microdeletion syndrome" @default.
- Q55786361 altLabel "Del(8)(p23.1)" @default.
- Q55786361 altLabel "Monosomy 8p23.1" @default.
- Q55786361 prefLabel "8p23.1 microdeletion syndrome" @default.
- Q55786361 P1550 Q55786361-81524A97-E4C9-47B6-865C-47364138F539 @default.
- Q55786361 P279 Q55786361-47C7DCD1-6FD6-457A-B1DF-5FF3783FF5E0 @default.
- Q55786361 P279 Q55786361-FD2D3104-D197-4C8C-8899-4A742AA79511 @default.
- Q55786361 P2888 Q55786361-16E3D580-0DED-4DB4-BE46-E6786EB99875 @default.
- Q55786361 P2892 Q55786361-8C0BE11D-B286-4CCE-905D-E813757ED091 @default.
- Q55786361 P31 Q55786361-2F5384E3-BA1B-4759-8369-A8A72AEA4113 @default.
- Q55786361 P31 Q55786361-809D4192-CB80-478A-985A-490C1EB09F5D @default.
- Q55786361 P4229 Q55786361-B0F2C11C-26A2-4918-A0EC-1BBF0699A7C7 @default.
- Q55786361 P486 Q55786361-839078CF-C19B-42D8-8E9F-B134AEB54ED6 @default.
- Q55786361 P5270 Q55786361-E474FFC0-44C1-4A26-8AD0-DAB694F40ED7 @default.
- Q55786361 P486 C537827 @default.
- Q55786361 P5270 MONDO_0016658 @default.
- Q55786361 P1550 "251071" @default.
- Q55786361 P279 Q55785600 @default.
- Q55786361 P279 Q55786593 @default.
- Q55786361 P2888 Orphanet_251071 @default.
- Q55786361 P2892 "C2931638" @default.
- Q55786361 P31 Q112193867 @default.
- Q55786361 P31 Q55788864 @default.
- Q55786361 P4229 "Q93.5" @default.
- Q55786361 P486 "C537827" @default.
- Q55786361 P5270 "MONDO_0016658" @default.