Osteogenesis imperfecta (Q46605): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Osteogênese imperfeita (OI) compreende um grupo heterogêneo de transtornos genéticos caracterizados por fragilidade óssea aumentada, baixa massa óssea e suscetibilidade a fraturas ósseas com gravidade variável. A característica clinicamente mais relevante de todos os tipos de OI é a fragilidade óssea, que se manifesta como múltiplas fraturas espontâneas.
@@ description / en / description / en @@
+Osteogenesis imperfecta (OI) comprises a heterogeneous group of genetic disorders characterised by increased bone fragility, low bone mass, and susceptibility to bone fractures with variable severity. The most clinically relevant characteristic of all types of OI is bone fragility, which manifests as multiple spontaneous fractures.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1219932551
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@@ Property / Canary Token: dki-india-LD24.K0 / rank @@
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@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
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@@ 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
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After 0
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++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 Q203
@@ Property / Linked ICD 10: ICD Q203 / rank @@
+Normal rank

Latest revision as of 15:18, 13 August 2026

Osteogenesis imperfecta (OI) comprises a heterogeneous group of genetic disorders characterised by increased bone fragility, low bone mass, and susceptibility to bone fractures with variable severity. The most clinically relevant characteristic of all types of OI is bone fragility, which manifests as multiple spontaneous fractures.

Language	Label	Description	Also known as
default for all languages	LD24.K0
English	Osteogenesis imperfecta	Osteogenesis imperfecta (OI) comprises a heterogeneous group of genetic disorders characterised by increased bone fragility, low bone mass, and susceptibility to bone fractures with variable severity. The most clinically relevant characteristic of all types of OI is bone fragility, which manifests as multiple spontaneous fractures.