Bent bone dysplasias (Q46624): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Quaisquer síndromes são caracterizadas por mineralização deficiente do crânio, craniossinostose, púbis e clavículas hipoplásicos, osteopenia, ossos longos curvados, orelhas de implantação baixa, hipertelorismo, hipoplasia da face média, dentes fetais erupcionados prematuramente e micrognatia. Essas síndromes podem estar associadas à mutação do gene FGFR2.
@@ description / en / description / en @@
+Any syndromes are characterised by poor mineralization of the skull, craniosynostosis, hypoplastic pubis and clavicles, osteopenia, bent long bones, low-set ears, hypertelorism, midface hypoplasia, prematurely erupted fetal teeth, and micrognathia. These syndromes may be associated with mutation of the FGFR2 gene.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/87260959
@@ Property / Canonical URI: https://id.who.int/icd/entity/87260959 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:LD24.C
@@ Property / CURIE: CID11:LD24.C / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-LD24.C
@@ Property / Canary Token: dki-india-LD24.C / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank
@@ Property / Linked ICD 10 @@
+ICD I391
@@ Property / Linked ICD 10: ICD I391 / rank @@
+Normal rank

Latest revision as of 15:20, 13 August 2026

Any syndromes are characterised by poor mineralization of the skull, craniosynostosis, hypoplastic pubis and clavicles, osteopenia, bent long bones, low-set ears, hypertelorism, midface hypoplasia, prematurely erupted fetal teeth, and micrognathia. These syndromes may be associated with mutation of the FGFR2 gene.

Language	Label	Description	Also known as
default for all languages	LD24.C
English	Bent bone dysplasias	Any syndromes are characterised by poor mineralization of the skull, craniosynostosis, hypoplastic pubis and clavicles, osteopenia, bent long bones, low-set ears, hypertelorism, midface hypoplasia, prematurely erupted fetal teeth, and micrognathia. These syndromes may be associated with mutation of the FGFR2 gene.