Q89.81ICD-10-CM 2027 · Billable
Kabuki syndrome
Sibling codes
Q89.89– Other specified congenital malformations
Inclusion terms
- Kabuki syndrome, type 1, due to KMT2D mutation
- Kabuki syndrome, type 2, due to KDM6A mutation
- Niikawa-Kuroki syndrome
Inherited from Q89.8: Other specified congenital malformations
Use additional code
- code(s) to identify all associated manifestations
Part of: Q89.8: Other specified congenital malformations › Q89: Other congenital malformations, not elsewhere classified