Congenital viral hepatitis (Q45758): Difference between revisions

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@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1270001765
@@ Property / Canonical URI: https://id.who.int/icd/entity/1270001765 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:KA62.9
@@ Property / CURIE: CID11:KA62.9 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-KA62.9
@@ Property / Canary Token: dki-india-KA62.9 / 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 @@
+P35.3
@@ Property / Linked ICD 10: P35.3 / rank @@
+Normal rank

Latest revision as of 13:57, 13 August 2026

A disease of the liver affecting the neonate, caused by an infection with either hepatitis A, B, C, D, or E virus in utero. This disease is characterised by lethargy, jaundice, abdominal distention, failure to thrive, or clay coloured stools. Transmission is by vertical transmission. Confirmation is by identification of the hepatitis A, B, C, D, or E virus in a blood sample from the neonate.

Language	Label	Description	Also known as
default for all languages	KA62.9
English	Congenital viral hepatitis	A disease of the liver affecting the neonate, caused by an infection with either hepatitis A, B, C, D, or E virus in utero. This disease is characterised by lethargy, jaundice, abdominal distention, failure to thrive, or clay coloured stools. Transmission is by vertical transmission. Confirmation is by identification of the hepatitis A, B, C, D, or E virus in a blood sample from the neonate.