SHMARQL

isolated trigonocephaly

<http://www.wikidata.org/entity/Q56014078>

Isolated trigonocephaly is a nonsyndromic form of craniosynostosis characterized by the premature fusion of the metopic suture
rdfs:label
"isolated trigonocephaly"@en
skos:altLabel "Non-syndromic metopic craniosynostosis"@en
"nonsyndromic trigonocephaly"@en
schema:description
"Isolated trigonocephaly is a nonsyndromic form of craniosynostosis characterized by the premature fusion of the metopic suture"@en
schema:dateModified "2026-10-24T00:09:19+00:00"^^xsd:dateTime
schema:version 2560162971
wikibase:identifiers 5
wikibase:sitelinks 0
wikibase:statements 21
p:P1193 wd:statement/Q56014078-B7EA87B8-23C8-4CE1-9DBE-07E05BA3CD9E
p:P14914 wd:statement/Q56014078-933E7664-0F82-41F6-982B-B886F5E60182
p:P1550 wd:statement/Q56014078-64866734-89EF-4FD3-B1DE-3D4DE463EA35
p:P2293 wd:statement/Q56014078-7F04C547-05F5-46A0-8AC7-2E2B14C96511
wd:statement/Q56014078-D95FCD19-126E-4C76-86AB-0D946001A3F2
p:P279 wd:statement/Q56014078-19eaf384-4c92-1bdf-01ee-7f6c41ef16a9
wd:statement/Q56014078-55DEB203-B970-4B74-86E1-A28AE280454B
p:P2841 wd:statement/Q56014078-3B819219-52D5-40E1-BEE3-E6C9A6D19C2E
wd:statement/Q56014078-472526C3-A456-44B3-8AF9-57DF564DC270
p:P2888 wd:statement/Q56014078-F9E7753E-D2DC-441D-B687-F969C1BAA4CB
p:P2892 wd:statement/Q56014078-AB4F8B21-E5DC-4181-9DEC-ABA3F49BA3C4
p:P31 wd:statement/Q56014078-1CDD7954-0C75-4BAE-AA5E-4B7005AE33FD
p:P4229 wd:statement/Q56014078-82CD8710-6C83-4861-B71F-459918809C7D
p:P5270 wd:statement/Q56014078-0FC39156-CDAC-40BB-B7C3-2D8D83D8F150
p:P6532 wd:statement/Q56014078-03DBFCB9-AD20-4D8A-AAF2-E60F14802EE6
wd:statement/Q56014078-27915E25-8B33-445B-A654-083482EE0FC3
wd:statement/Q56014078-5A8A0971-BD9D-488D-A9DB-7B27C0C28BF3
wd:statement/Q56014078-64428350-1034-4D24-8E3B-2B32157B93B8
wd:statement/Q56014078-689A2402-E157-4F61-9AA0-F2E30EB1FEFA
wd:statement/Q56014078-BF3710E2-B9B7-43FB-B452-8B6D3133F323
wd:statement/Q56014078-CA75B667-7C6E-489A-A44D-FB1326278CC7
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0018065>
wdt:P1193 0.0003^^xsd:decimal
wdt:P14914 "D03366"
wdt:P1550 "3366"
wdt:P2293 FGFR1
FREM1
wdt:P279 trigonocephaly
isolated craniosynostosis
wdt:P2841 neonatal onset
infantile onset
wdt:P2888 <http://www.orpha.net/ORDO/Orphanet_3366>
wdt:P2892 "C0265535"
wdt:P31 type of disease
wdt:P4229 "Q75.0"
wdt:P5270 "MONDO_0018065"
wdt:P6532 Synophrys
omphalocele
intracranial hypertension
developmental language disorder
craniosynostosis
Hypotelorism
papilledema
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