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CIM11 LD2H.3

CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-11

Waardenburg-Shah syndrome

chapitre
20 Developmental anomalies
bloc
Multiple developmental anomalies or syndromes
definition
In this syndrome the phenotype includes not only the classical features of Waardenburg syndrome but also Hirschsprung disease. It may be caused by mutations in SOX10, EDN3 or EDNRB genes.
type
category
navigateur oms (fr)
https://icd.who.int/browse/2026-01/mms/fr#1420151003 ↗