Matches in Wikidata for { <http://www.wikidata.org/entity/Q56013735> ?p ?o ?g. }
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- Q56013735 description "The 2p21 microdeletion syndrome consists of cystinuria, neonatal seizures, hypotonia, severe growthand developmental delay, facial dysmorphism, and lactic acidemia" @default.
- Q56013735 name "2p21 microdeletion syndrome" @default.
- Q56013735 name "Síndrome de microdeleción 2p21" @default.
- Q56013735 type Item @default.
- Q56013735 label "2p21 microdeletion syndrome" @default.
- Q56013735 label "Síndrome de microdeleción 2p21" @default.
- Q56013735 altLabel "2p21 deletion syndrome" @default.
- Q56013735 altLabel "2p21 deletion" @default.
- Q56013735 altLabel "Del(2)(p21)" @default.
- Q56013735 altLabel "Monosomy 2p21" @default.
- Q56013735 prefLabel "2p21 microdeletion syndrome" @default.
- Q56013735 prefLabel "Síndrome de microdeleción 2p21" @default.
- Q56013735 P1550 Q56013735-244E3E42-082D-4860-9882-ACFB2491B08F @default.
- Q56013735 P279 Q56013735-fd7ca791-460a-298a-011e-f80b3def62e2 @default.
- Q56013735 P2888 Q56013735-77E20EC0-A783-425A-8993-1634D905E3B8 @default.
- Q56013735 P2892 Q56013735-84433290-BED9-4131-9200-C1A3D562D9D0 @default.
- Q56013735 P31 Q56013735-5181AD18-DA7E-4F53-A941-71BBBEC48A0F @default.
- Q56013735 P4229 Q56013735-E7EDA536-3F51-4CDC-9A17-CC533A0E074F @default.
- Q56013735 P5270 Q56013735-83224353-110F-467C-ABB7-C2AFC16DB424 @default.
- Q56013735 P7807 Q56013735-d0ea805a-4510-3702-2ac8-aa0677d347cd @default.
- Q56013735 P5270 MONDO_0015583 @default.
- Q56013735 P1550 "163693" @default.
- Q56013735 P279 Q55786588 @default.
- Q56013735 P2888 Orphanet_163693 @default.
- Q56013735 P2892 "C4304537" @default.
- Q56013735 P31 Q112193867 @default.
- Q56013735 P4229 "Q93.5" @default.
- Q56013735 P5270 "MONDO_0015583" @default.
- Q56013735 P7807 "1956669459" @default.