Matches in Wikidata for { <http://www.wikidata.org/entity/Q55785689> ?p ?o ?g. }
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- Q55785689 description "This syndrome associates gingival fibromatosis with dental abnormalities including generalized thin hypoplastic amelogenesis imperfecta, intrapulpal calcifications, and delay of tooth eruption" @default.
- Q55785689 name "amelogenesis imperfecta-gingival hyperplasia syndrome" @default.
- Q55785689 type Item @default.
- Q55785689 label "amelogenesis imperfecta-gingival hyperplasia syndrome" @default.
- Q55785689 prefLabel "amelogenesis imperfecta-gingival hyperplasia syndrome" @default.
- Q55785689 P1550 Q55785689-F6ACB6BC-F579-4CE9-B002-4D815DBF9BCD @default.
- Q55785689 P279 Q55785689-4f80c278-43ad-1a76-6c74-a0bca9afd5f7 @default.
- Q55785689 P279 Q55785689-911B34FE-AAEA-4772-ACD0-5215125F95FA @default.
- Q55785689 P2888 Q55785689-58F4FD92-1E89-4A81-9488-2C47FCBE2ACB @default.
- Q55785689 P31 Q55785689-512E4B6C-7193-4347-AC67-094933C27F85 @default.
- Q55785689 P4229 Q55785689-555DA2ED-108E-456C-9E16-3901F749BE91 @default.
- Q55785689 P492 Q55785689-67AD4924-88FD-48A4-A19A-9952F3F652A8 @default.
- Q55785689 P5270 Q55785689-F6B2A9DE-680B-4FF8-B40A-FE8593850B2C @default.
- Q55785689 P5270 MONDO_0015750 @default.
- Q55785689 P1550 "171836" @default.
- Q55785689 P279 Q461854 @default.
- Q55785689 P279 Q55788118 @default.
- Q55785689 P2888 Orphanet_171836 @default.
- Q55785689 P31 Q112193867 @default.
- Q55785689 P4229 "K00.5" @default.
- Q55785689 P492 "614253" @default.
- Q55785689 P5270 "MONDO_0015750" @default.