Matches in Wikidata for { <http://www.wikidata.org/entity/Q55787032> ?p ?o ?g. }
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- Q55787032 description "1p21.3 microdeletion syndrome is an extremely rare chromosomal anomaly characterized by severe speech and language delay, intellectual deficiency, autism spectrum disorder(see this term)." @default.
- Q55787032 name "1p21.3 microdeletion syndrome" @default.
- Q55787032 type Item @default.
- Q55787032 label "1p21.3 microdeletion syndrome" @default.
- Q55787032 altLabel "Del(1)p(21.3)" @default.
- Q55787032 altLabel "Monosomy 1p21.3" @default.
- Q55787032 prefLabel "1p21.3 microdeletion syndrome" @default.
- Q55787032 P1550 Q55787032-168CFB3A-BDEB-45A9-A457-1094C94E3B0E @default.
- Q55787032 P279 Q55787032-0AB2DEC0-2DE5-4DB2-A472-057CADD61C16 @default.
- Q55787032 P279 Q55787032-EAAFA9E2-6664-4FF7-A95A-D618A1ED9AAA @default.
- Q55787032 P279 Q55787032-F17BCE19-C2EA-4B6F-B475-520B56ED9B42 @default.
- Q55787032 P2888 Q55787032-8A331FCC-0397-4000-B1AC-2B3FB812B9D2 @default.
- Q55787032 P2892 Q55787032-C75FCFA8-BB56-49DB-BDA1-8F913FF740CC @default.
- Q55787032 P31 Q55787032-3B655BF3-51AD-4CE9-B375-A3DDD63C6097 @default.
- Q55787032 P31 Q55787032-4776734A-CC1D-4D8B-9378-BD42651AF212 @default.
- Q55787032 P4229 Q55787032-FE708BF7-9B0B-431B-9694-A284E798D6BB @default.
- Q55787032 P5270 Q55787032-60EEB8F2-E87A-409B-B27A-FD56D0D45AAB @default.
- Q55787032 P5270 MONDO_0017405 @default.
- Q55787032 P1550 "293948" @default.
- Q55787032 P279 Q55785790 @default.
- Q55787032 P279 Q55785866 @default.
- Q55787032 P279 Q55786587 @default.
- Q55787032 P2888 Orphanet_293948 @default.
- Q55787032 P2892 "C4304578" @default.
- Q55787032 P31 Q112193867 @default.
- Q55787032 P31 Q55788864 @default.
- Q55787032 P4229 "Q93.5" @default.
- Q55787032 P5270 "MONDO_0017405" @default.