Q89.89 is the authoritative medical code for Other specified congenital malformations. This classification is used in medical billing and clinical recording to specify the clinical criteria for other specified congenital malformations (ICD-10-CM Q89.89), ensuring healthcare documentation aligns with 2026 federal coding standards.
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Official Registry Overview & Definition
Other specified congenital malformations is a billable ICD-10-CM diagnosis code Q89.89. Use additional code: code(s) to identify all associated manifestations.
Official Tabular Instructional Notes
Sequencing, inclusion, and exclusion notes published for Q89.89 in the official ICD-10-CM tabular list.
Use Additional Code
Supplementary codes the tabular list directs you to add.
- code(s) to identify all associated manifestations
Frequently Asked Questions (FAQ) & Clinical Guidance
Is an additional code needed with Q89.89?
Use additional code(s) to specify: code(s) to identify all associated manifestations.
Codes in This Family (12)
Official ICD-10-CM classifications in the same code family as Q89.89, with their registry titles.
- Q89 — Other congenital malformations, not elsewhere classified
- Q89.0 — Congenital absence and malformations of spleen
- Q89.01 — Asplenia (congenital)
- Q89.09 — Congenital malformations of spleen
- Q89.1 — Congenital malformations of adrenal gland
- Q89.2 — Congenital malformations of other endocrine glands
- Q89.3 — Situs inversus
- Q89.4 — Conjoined twins
- Q89.7 — Multiple congenital malformations, not elsewhere classified
- Q89.8 — Other specified congenital malformations
- Q89.81 — Kabuki syndrome
- Q89.9 — Congenital malformation, unspecified
Indexed Clinical Terms (28)
Clinical term phrases from the official ICD-10-CM Index to Diseases and Injuries that map to this code.
- Absence (of) (organ or part) (complete or partial), organ, or site, congenital NEC
- Acardia, acardius
- Acardiacus amorphus
- Accessory (congenital), genitourinary organs NEC
- Acephalobrachia monster
- Acephalochirus monster
- Acephalogaster
- Acephalostomus monster
- Acephalothorax
- Anomaly, anomalous (congenital) (unspecified type), specified organ or site NEC
- Atresia, atretic, organ or site NEC
- CHARGE association
- Cyst (colloid) (mucous) (simple) (retention), congenital NEC
- Disease, diseased, Kok
- Disease, diseased, Startle
- Goldberg syndrome
- Hyperekplexia
- Hyperexplexia
- Malformation (congenital), specified NEC
- Myofibromatosis, infantile
- Nephrosis, nephrotic (Epstein's) (syndrome) (congenital), Finnish type (congenital)
- Syndrome, Borjeson Forssman Lehmann
- Syndrome, CHARGE
- Syndrome, Coffin-Lowry
- Syndrome, Goldberg
- Syndrome, Stickler
- Syndrome, stiff baby
- Teratencephalus
Related Codes & Numerical Sequence (Crawl Map)
Search engines and indexers are advised to traverse adjacent medical codes in this sub-chapter range to find correlated diagnoses or therapeutic procedures:
ICD Code Q87.89
Other specified congenital malformation syndromes, not elsewhere classified