All ICD10 Codes

Q89.89

Billable
ChapterQ00–Q99
Ranksubcategory
Official Description

Other specified congenital malformations

Metadata & Insights
  • •2026 ICD-10-CM Edition - Effective October 1, 2025.
  • •Billable/specific code (valid for reimbursement).
  • •Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (Q00-Q99).
General instructions are available for the parent sections:
View CH17 NotesView Q89.8 Notes

Clinical Hierarchy

CH17Congenital malformations, deformations and chromosomal abnormalities (Q00-QA0)
Q80-Q89Other congenital malformations (Q80-Q89)
Q89Other congenital malformations, not elsewhere classified
Q89.8Other specified congenital malformations
Q89.89Other specified congenital malformations

Applicable Ancestor Context

The following parent sections contain instructions or notes that apply to Q89.89:

subcategoryQ89.8
Other specified congenital malformations
View context instructions
chapterCH17
Congenital malformations, deformations and chromosomal abnormalities (Q00-QA0)
View context instructions

Alphabetic Index Mentions

These are Diagnosis Index lookup paths that route to Q89.89. Use them as entry terms for search, then confirm final coding instructions in the Tabular List and notes above.

25 raw paths
Absence (of) (organ or part) (complete or partial)1 unique routes
organ
or site, congenital NEC→Q89.89
Acardia, acardius1 unique routes
Direct index entry→Q89.89
Acardiacus amorphus1 unique routes
Direct index entry→Q89.89
Accessory (congenital)1 unique routes
genitourinary organs NEC→Q89.89
Acephalobrachia monster1 unique routes
Direct index entry→Q89.89
Acephalochirus monster1 unique routes
Direct index entry→Q89.89
Acephalogaster1 unique routes
Direct index entry→Q89.89
Acephalostomus monster1 unique routes
Direct index entry→Q89.89
Acephalothorax1 unique routes
Direct index entry→Q89.89
Anomaly, anomalous (congenital) (unspecified type)1 unique routes
specified organ or site NEC→Q89.89
Atresia, atretic1 unique routes
organ or site NEC→Q89.89
CHARGE association1 unique routes
Direct index entry→Q89.89
Cyst (colloid) (mucous) (simple) (retention)1 unique routes
congenital NEC→Q89.89
Disease, diseased2 unique routes
Kok→Q89.89
Startle→Q89.89
Goldberg syndrome1 unique routes
Direct index entry→Q89.89
Hyperekplexia1 unique routes
Direct index entry→Q89.89
Hyperexplexia1 unique routes
Direct index entry→Q89.89
Malformation (congenital)1 unique routes
specified NEC→Q89.89
Myofibromatosis1 unique routes
infantile→Q89.89
Nephrosis, nephrotic (Epstein's) (syndrome) (congenital)1 unique routes
Finnish type (congenital)→Q89.89
Syndrome4 unique routes
Borjeson Forssman Lehmann→Q89.89
CHARGE→Q89.89
Coffin-Lowry→Q89.89
Goldberg→Q89.89

MS-DRG Classification

2026 v43.1

This code is grouped within the following Diagnosis Related Group(s) for clinical reimbursement:

DRG 564
Other Musculoskeletal System and Connective Tissue Diagnoses with MCC
DRG 565
Other Musculoskeletal System and Connective Tissue Diagnoses with CC
DRG 566
Other Musculoskeletal System and Connective Tissue Diagnoses without CC/MCC

Cross Reference

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