Q89.89
Other specified congenital malformations
Billable FY2026 2025-10-01 → 2026-09-30
FY2026–2027 only
Instructional notes 1
Q89.8code
Use additional code
- code(s) to identify all associated manifestations
Index entries leading here 22
- Absence (of) (organ or part) (complete or partial)
- organ
- or site, congenital NEC Q89.89
- organ
- Acardia, acardius Q89.89
- Acardiacus amorphus Q89.89
- Accessory (congenital)
- genitourinary organs NEC Q89.89
- Acephalobrachia monster Q89.89
- Acephalochirus monster Q89.89
- Acephalogaster Q89.89
- Acephalostomus monster Q89.89
- Acephalothorax Q89.89
- Anomaly, anomalous (congenital) (unspecified type) Q89.9
- specified organ or site NEC Q89.89
- Atresia, atretic
- organ or site NEC Q89.89
- Syndrome — see also Disease
- CHARGE association Q89.89
- Cyst (colloid) (mucous) (simple) (retention)
- congenital NEC Q89.89
- Disease, diseased — see also Syndrome
- Nephrosis, nephrotic (Epstein's) (syndrome) (congenital) N04.9
- Finnish type (congenital) Q89.89
- Goldberg syndrome Q89.89
- Hyperekplexia Q89.89
- Hyperexplexia Q89.89
- Myofibromatosis D48.19
- infantile Q89.89
- Malformation (congenital) — see also Anomaly
- specified NEC Q89.89
- Teratencephalus Q89.89
Alongside this code 1 same parent — Q89.8
Additional references
AHA Coding Clinic® Licence required
Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.