Q89.9
BillableCongenital malformation, unspecified
Congenital malformation, unspecified
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital anomaly NOS
- Congenital deformity NOS
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(7)
Q89.0Congenital absence and malformations of spleen
Q89.1Congenital malformations of adrenal gland
Q89.2Congenital malformations of other endocrine glands
Q89.3Situs inversus
Q89.4Conjoined twins
Q89.7Multiple congenital malformations, not elsewhere classified
Q89.8Other specified congenital malformations
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(195)
SNOMED CT
- Congenital cerebral porosis38353004
- Congenital porencephalia38353004
- Congenital porencephaly38353004
- Schizencephalic porencephaly38353004
- Chicken breast38774000
- Keeled chest38774000
- Pectus carinatum38774000
- Pigeon breast38774000
- Pigeon chest38774000
- Congenital disease66091009
- Congenital disorder66091009
- Congenital abnormal shape of rib92943002
- Congenital misshapen rib92943002
- Mis-shapen ribs92943002
- Malformation sequence105989001
- Congenital pectus carinatum205101001
- Amegakaryocytic thrombocytopenia234482009
- CM - Congenital malformation276654001
- Congenital abnormality276654001
- Congenital anomaly276654001
- Congenital malformation276654001
- Fetal developmental abnormality276654001
- Fetal malformation276654001
- Foetal developmental abnormality276654001
- Foetal malformation276654001
- Congenital deformity276655000
- Birth defect276720006
- Dysmorphia276720006
- Dysmorphism276720006
- Deformity of sternum298727009
- Amegakaryocytic thrombocytopenia with congenital malformation359531004
- Congenital anomaly of back363025000
- Congenital sequelae of disorders363042006
- Congenital malformation syndrome400038003
- Multiple congenital anomalies400038003
- Multiple congenital malformations400038003
- Deformity417893002
- Pectus deformity of chest444693004
- Single congenital anomaly698601005
- Single congenital malformation698601005
- Congenital anomaly of mother complicating pregnancy721153000
- Maternal congenital anomaly complicating pregnancy721153000
- Spinocerebellar ataxia dysmorphism syndrome733033001
- Dysmorphism, pectus carinatum, joint laxity syndrome733038005
- Guízar Vázquez Sánchez Manzano syndrome733038005
- Dysmorphism, short stature, deafness, disorder of sex development syndrome733050004
- Dysmorphism, short stature, deafness, pseudohermaphroditism syndrome733050004
- Bonnemann Meinecke syndrome763821001
- Porencephaly, cerebellar hypoplasia, internal malformations syndrome763821001
- Pulmonary hypertension due to developmental abnormality1010627004
UMLS
- ABNORM CONGENC0000768
- AbnormalitiesC0000768
- Abnormalities, CongenitalC0000768
- Abnormality, CongenitalC0000768
- Anomaly congenitalC0000768
- Birth DefectC0000768
- Birth DefectsC0000768
- Birth defectsC0000768
- CM - Congenital malformationC0000768
- CONGEN ABNORMC0000768
- CONGEN DEFECTSC0000768
- Congenital AbnormalitiesC0000768
- Congenital AbnormalityC0000768
- Congenital Anatomic AbnormalityC0000768
- Congenital Anatomical AbnormalityC0000768
- Congenital AnomalyC0000768
- Congenital Anomaly or Birth DefectC0000768
- Congenital DefectC0000768
- Congenital DefectsC0000768
- Congenital DeformityC0000768
- Congenital MalformationC0000768
- Congenital abnormalityC0000768
- Congenital abnormality NOSC0000768
- Congenital anomalyC0000768
- Congenital anomaly NOSC0000768
- Congenital deformityC0000768
- Congenital deformity (disorder)C0000768
- Congenital deformity NOSC0000768
- Congenital malformationC0000768
- Congenital malformation (disorder)C0000768
- Congenital malformation, unspecifiedC0000768
- DEFECTS CONGENC0000768
- Defect, BirthC0000768
- Defect, CongenitalC0000768
- Defects, CongenitalC0000768
- DeformitiesC0000768
- DeformityC0000768
- Developmental disturbanceC0000768
- Fetal anomalyC0000768
- Fetal developmental abnormalityC0000768
- Fetal malformationC0000768
- Foetal developmental abnormalityC0000768
- Foetal malformationC0000768
- abnormal developmentC0000768
- birth defectC0000768
- birth defectsC0000768
- congenital abnormalitiesC0000768
- congenital abnormalityC0000768
- congenital anomaliesC0000768
- congenital anomalyC0000768
- congenital defectC0000768
- congenital defectsC0000768
- congenital deformityC0000768
- congenital malformationC0000768
- congenital malformationsC0000768
- deformityC0000768
- developmental defectC0000768
- dysgenesisC0000768
- dysmorphismC0000768
- dysmorphismsC0000768
- fetal anomalyC0000768
- fetal malformationC0000768
- malformationC0000768
Clinical Terms
- Deformity of sternum
- Abnormality, Congenital
- Congenital disorder
- CONGEN ABNORM
- Amegakaryocytic thrombocytopenia
- Abnormalities
- Multiple congenital anomalies
- Foetal developmental abnormality
- Congenital Deformity
- dysgenesis
- congenital defect
- malformation
- Foetal malformation
- Congenital porencephalia
- Deformity
- Congenital Anomaly
- Single congenital malformation
- Bonnemann Meinecke syndrome
- Congenital misshapen rib
- Congenital anomaly of back
- Pectus deformity of chest
- Amegakaryocytic thrombocytopenia with congenital malformation
- Multiple congenital malformations
- fetal malformation
- abnormal development
- Birth defects
- Congenital abnormal shape of rib
- dysmorphisms
- Porencephaly, cerebellar hypoplasia, internal malformations syndrome
- Congenital anomaly of mother complicating pregnancy
- congenital abnormality
- Congenital pectus carinatum
- congenital abnormalities
- Congenital cerebral porosis
- Fetal anomaly
- Spinocerebellar ataxia dysmorphism syndrome
- Deformities
- Congenital deformity (disorder)
- Congenital Anatomical Abnormality
- Mis-shapen ribs
- Congenital malformation syndrome
- Maternal congenital anomaly complicating pregnancy
- DEFECTS CONGEN
- CM - Congenital malformation
- Pectus carinatum
- Congenital deformity NOS
- Anomaly congenital
- Keeled chest
- Congenital disease
- Dysmorphism
- Congenital malformation (disorder)
- Congenital Anatomic Abnormality
- congenital defects
- Dysmorphism, pectus carinatum, joint laxity syndrome
- Dysmorphism, short stature, deafness, disorder of sex development syndrome
- congenital malformations
- Congenital porencephaly
- Birth Defect
- Defect, Congenital
- Pulmonary hypertension due to developmental abnormality
- CONGEN DEFECTS
- Congenital Anomaly or Birth Defect
- Single congenital anomaly
- Defect, Birth
- developmental defect
- congenital anomalies
- Guízar Vázquez Sánchez Manzano syndrome
- Fetal developmental abnormality
- Chicken breast
- Defects, Congenital
- Malformation sequence
- Congenital anomaly NOS
- Congenital abnormality NOS
- Abnormalities, Congenital
- Schizencephalic porencephaly
- Dysmorphia
- Pigeon chest
- Dysmorphism, short stature, deafness, pseudohermaphroditism syndrome
- ABNORM CONGEN
- Congenital sequelae of disorders
- Pigeon breast
- Developmental disturbance
Frequently Asked Questions
What is the ICD-10 code for congenital malformation, unspecified?
The ICD-10-CM code for congenital malformation, unspecified is Q89.9. The full clinical description is "Congenital malformation, unspecified". Q89.9 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q89.9 mean?
ICD-10-CM code Q89.9 represents “Congenital malformation, unspecified”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q89.9 a billable code?
Yes, Q89.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q89.9 in?
Q89.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q89.9 map to?
Q89.9 maps to 24 SNOMED CT concepts: 234482009, 359531004, 276720006, 763821001, 276654001, and 19 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q89.9?
Q89.9 is linked to 1 UMLS Concept Unique Identifier: C0000768. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q89.9 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformation, unspecified affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of Q89.9?
Q89.9 maps to the ICD-11 code: LD9Z (Developmental anomalies, unspecified).
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.