Q89.89
Other specified congenital malformations
Billable code
This code does not map to a risk-adjusting HCC in the loaded models.
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
Inherited from Q89.8Other specified congenital malformations
Use additional
code(s) to identify all associated manifestations
Inherited from chapter 17Congenital malformations, deformations and chromosomal abnormalities
Excludes 2
inborn errors of metabolism (E70-E88)
Official Guidelines for Q89.89
FY 2026 ›Sections that reference Q89.89
Sections whose FY 2026 text names Q89.89, its Q89 category, or a range containing it — the chapter guidance above is the authoritative source.
Find Q89.89 in the alphabetic index
25 index paths lead to this code
- Acardia, acardius
- Acardiacus amorphus
- Acephalobrachia monster
- Acephalochirus monster
- Acephalogaster
- Acephalostomus monster
- Acephalothorax
- CHARGE association
- Goldberg syndrome
- Hyperekplexia
- Hyperexplexia
- Teratencephalus
- Accessory › genitourinary organs NEC
- Anomaly, anomalous › specified organ or site NEC
- Atresia, atretic › organ or site NEC
- Cyst › congenital NEC
- Disease, diseased › Kok
- Disease, diseased › Startle
- Malformation › specified NEC
- Myofibromatosis › infantile
- Nephrosis, nephrotic › Finnish type
- Syndrome › Borjeson Forssman Lehmann
- Syndrome › CHARGE
- Syndrome › Coffin-Lowry
- Syndrome › Goldberg