Opsismodysplasia (Q86546): Difference between revisions

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+https://id.who.int/icd/entity/2147268863
@@ Property / Canonical URI: https://id.who.int/icd/entity/2147268863 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_2147268863
@@ Property / CURIE: CID11:ID_2147268863 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_2147268863
@@ Property / Canary Token: dki-india-ID_2147268863 / rank @@
+Normal rank
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+Concluído
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@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
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+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
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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

Latest revision as of 11:57, 15 August 2026

Opsismodysplasia is a skeletal dysplasia characterised by congenital dwarfism (rhizomelic micromelia) and facial dysmorphism (macrocephaly, prominent brow, large fontanels, depressed nasal bridge, a small nose, anteverted nares and a long philtrum, hypertelorism, and exophthalmos).

Language	Label	Description	Also known as
default for all languages	ID_2147268863
English	Opsismodysplasia	Opsismodysplasia is a skeletal dysplasia characterised by congenital dwarfism (rhizomelic micromelia) and facial dysmorphism (macrocephaly, prominent brow, large fontanels, depressed nasal bridge, a small nose, anteverted nares and a long philtrum, hypertelorism, and exophthalmos).