KBG syndrome (Q94173): Difference between revisions

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+https://id.who.int/icd/entity/465550090
@@ Property / Canonical URI: https://id.who.int/icd/entity/465550090 / rank @@
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@@ Property / CURIE: CID11:ID_465550090 / rank @@
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@@ Property / Canary Token: dki-india-ID_465550090 / rank @@
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@@ Property / Knowledge Architect @@
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+August 2026Timestamp +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
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After 0
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++2026-08-15T00:00:00Z
-Timezone
++00:00
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@@ Property / Collection date: 15 August 2026 / rank @@
+Normal rank

Latest revision as of 09:18, 16 August 2026

KBG syndrome is a rare malformation syndrome characterised by a typical facial dysmorphism, macrodontia of the upper central incisors, skeletal (mainly costovertebral) anomalies and developmental delay.

Language	Label	Description	Also known as
default for all languages	ID_465550090
English	KBG syndrome	KBG syndrome is a rare malformation syndrome characterised by a typical facial dysmorphism, macrodontia of the upper central incisors, skeletal (mainly costovertebral) anomalies and developmental delay.