Q67.5
BillableCongenital deformity of spine
Congenital deformity of spine
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital postural scoliosis
- Congenital scoliosis NOS
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(8)
Q67.0Congenital facial asymmetry
Q67.1Congenital compression facies
Q67.2Dolichocephaly
Q67.3Plagiocephaly
Q67.4Other congenital deformities of skull, face and jaw
Q67.6Pectus excavatum
Q67.7Pectus carinatum
Q67.8Other congenital deformities of chest
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(177)
SNOMED CT
- Macrodactyly of toe4136000
- Macroencephaly9740002
- Megalencephaly9740002
- Bilateral congenital dislocation of hip10155006
- Congenital postural scoliosis20944008
- Congenital scoliosis20944008
- Cutis laxa, autosomal recessive59451000
- Congenital humpback71311003
- Congenital hunchback71311003
- Congenital kyphosis71311003
- Congenital elevation of scapula79120002
- Sprengel's deformity79120002
- Undescended shoulder79120002
- Lordoscoliosis deformity of spine111268000
- Lordosis and scoliosis deformity of spine111268000
- Compensatory scoliosis203645000
- Postural scoliosis203645000
- Congenital deformity of spine205043005
- Congenital overgrowth of foot205372002
- Hip pathological dislocation239759009
- Congenital kyphoscoliosis405772002
- Ehlers-Danlos syndrome kyphoscoliotic type718211004
- Ehlers-Danlos syndrome type 6718211004
- Ehlers-Danlos syndrome type VI718211004
- Giuffre Tsukahara syndrome719162001
- Radioulnar synostosis with microcephaly and scoliosis syndrome719162001
- Tsukahara syndrome719162001
- Microcephalus with brachydactyly and kyphoscoliosis syndrome719378009
- Microcephaly with brachydactyly and kyphoscoliosis syndrome719378009
- Viljoen Kallis Voges syndrome719378009
- CATSHL (camptodactyly, tall stature, scoliosis, hearing loss) syndrome720601000
- Camptodactyly and tall stature with scoliosis and hearing loss syndrome720601000
- Ehlers-Danlos syndrome kyphoscoliotic and deafness type720859009
- Ehlers-Danlos syndrome kyphoscoliotic and hearing loss type720859009
- Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and deafness720859009
- Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency720859009
- Ferlini Ragno Calzolari syndrome721229003
- Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome721229003
- Waaler Aarskog syndrome721229003
- MACS (macrocephaly, alopecia, cutis laxa, scoliosis) syndrome723367005
- MACS syndrome723367005
- Macrocephaly, alopecia, cutis laxa, scoliosis syndrome723367005
- RIN2 deficiency723367005
- Tall forehead, sparse hair, skin hyperextensibility, scoliosis syndrome723367005
- Congenital dislocation of left hip767002009
- Congenital dislocation of right hip767003004
- Tall stature, scoliosis, macrodactyly of great toe syndrome770788000
- Tall stature, scoliosis, macrodactyly of hallux syndrome770788000
- Acrodysplasia scoliosis773773006
- Brachydactyly, scoliosis, carpal fusion syndrome773773006
- Prata Liberal Goncalves syndrome773773006
- SSM (seizures, scoliosis, macrocephaly) syndrome1187250005
- Seizures, scoliosis, macrocephaly syndrome1187250005
- Congenital lordosis deformity of spine1187358001
- Congenital lordoscoliosis deformity of spine1187359009
- Congenital lordosis and scoliosis deformity of spine1187359009
- Bilateral hip and radial head dislocations, short stature, scoliosis, carpal coalition, pes cavus, facial dysmorphism syndrome1197589000
- Steel syndrome1197589000
- Megalencephaly, severe kyphoscoliosis, overgrowth syndrome1260143005
- Congenital radioulnar synostosis1268409009
- Pathological dislocation of bilateral hips15720721000119105
- Pathological dislocation of left hip15720681000119104
- Pathological dislocation of right hip15720761000119100
UMLS
- Congenital Postural ScoliosisC0265675
- Congenital postural scoliosisC0265675
- Congenital postural scoliosis (disorder)C0265675
- Congenital anomalies of spineC0158775
- Congenital anomaly of spineC0158775
- Congenital anomaly of spine (disorder)C0158775
- Congenital anomaly of vertebral columnC0158775
- Congenital deformity of spineC0158775
- Congenital deformity of spine (disorder)C0158775
- Congenital malformation of spineC0158775
- Congenital malformation of spine NOSC0158775
- Congenital spine malformationC0158775
- Congenital spine malformation NOSC0158775
- Malformation of spine NOSC0158775
- Spine malformationC0158775
- Spine malformation NOSC0158775
- Vertebral malformationsC0158775
- anomalies spineC0158775
- anomaly spineC0158775
- congenital deformities spineC0158775
- malformation spineC0158775
- malformations spineC0158775
- spine malformationC0158775
- Congenital scoliosisC0559260
- Congenital scoliosis NOSC0559260
- Scoliosis, congenitalC0559260
- congenital scoliosisC0559260
- inborn lateral curvature of the spineC0559260
- inborn scoliosisC0559260
Clinical Terms
- Pathological dislocation of right hip
- Congenital scoliosis NOS
- CATSHL (camptodactyly, tall stature, scoliosis, hearing loss) syndrome
- Congenital deformity of spine (disorder)
- Congenital anomalies of spine
- Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and deafness
- Congenital elevation of scapula
- Compensatory scoliosis
- malformations spine
- Congenital anomaly of spine (disorder)
- Congenital malformation of spine NOS
- Vertebral malformations
- Congenital dislocation of left hip
- Congenital Postural Scoliosis
- Cutis laxa, autosomal recessive
- MACS syndrome
- Brachydactyly, scoliosis, carpal fusion syndrome
- Sprengel's deformity
- Congenital anomaly of vertebral column
- Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome
- congenital deformities spine
- Spine malformation NOS
- Congenital humpback
- Giuffre Tsukahara syndrome
- Congenital anomaly of spine
- Pathological dislocation of left hip
- Congenital kyphoscoliosis
- inborn lateral curvature of the spine
- Prata Liberal Goncalves syndrome
- Congenital lordosis deformity of spine
- Malformation of spine NOS
- RIN2 deficiency
- congenital scoliosis
- Congenital lordoscoliosis deformity of spine
- Congenital overgrowth of foot
- inborn scoliosis
- MACS (macrocephaly, alopecia, cutis laxa, scoliosis) syndrome
- Scoliosis, congenital
- Radioulnar synostosis with microcephaly and scoliosis syndrome
- Congenital dislocation of right hip
- Tsukahara syndrome
- Congenital radioulnar synostosis
- spine malformation
- SSM (seizures, scoliosis, macrocephaly) syndrome
- Bilateral hip and radial head dislocations, short stature, scoliosis, carpal coalition, pes cavus, facial dysmorphism syndrome
- Congenital malformation of spine
- Microcephalus with brachydactyly and kyphoscoliosis syndrome
- Macrodactyly of toe
- Camptodactyly and tall stature with scoliosis and hearing loss syndrome
- Acrodysplasia scoliosis
- Congenital lordosis and scoliosis deformity of spine
- anomalies spine
- Congenital spine malformation NOS
- Undescended shoulder
- Postural scoliosis
- Hip pathological dislocation
- Steel syndrome
- Congenital hunchback
- Congenital kyphosis
- Ehlers-Danlos syndrome type 6
- Tall stature, scoliosis, macrodactyly of great toe syndrome
- Macroencephaly
- Lordoscoliosis deformity of spine
- malformation spine
- Tall stature, scoliosis, macrodactyly of hallux syndrome
- Ehlers-Danlos syndrome kyphoscoliotic and hearing loss type
- Tall forehead, sparse hair, skin hyperextensibility, scoliosis syndrome
- Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency
- Viljoen Kallis Voges syndrome
- Ferlini Ragno Calzolari syndrome
- anomaly spine
- Microcephaly with brachydactyly and kyphoscoliosis syndrome
- Congenital spine malformation
- Macrocephaly, alopecia, cutis laxa, scoliosis syndrome
- Pathological dislocation of bilateral hips
- Waaler Aarskog syndrome
- Seizures, scoliosis, macrocephaly syndrome
- Congenital postural scoliosis (disorder)
- Megalencephaly
- Megalencephaly, severe kyphoscoliosis, overgrowth syndrome
- Bilateral congenital dislocation of hip
- Ehlers-Danlos syndrome kyphoscoliotic and deafness type
- Lordosis and scoliosis deformity of spine
- Ehlers-Danlos syndrome type VI
- Ehlers-Danlos syndrome kyphoscoliotic type
Frequently Asked Questions
What is the ICD-10 code for congenital deformity of spine?
The ICD-10-CM code for congenital deformity of spine is Q67.5. The full clinical description is "Congenital deformity of spine". Q67.5 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q67.5 mean?
ICD-10-CM code Q67.5 represents “Congenital deformity of spine”. 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 Q67.5 a billable code?
Yes, Q67.5 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q67.5 in?
Q67.5 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q67.5?
Q67.5 has Excludes1 notes indicating codes that cannot be used together with it, including: congenital malformation syndromes classified to Q87.-; Potter's syndrome (Q60.6); infantile idiopathic scoliosis (M41.0); and 1 more.
What SNOMED CT codes does Q67.5 map to?
Q67.5 maps to 33 SNOMED CT concepts: 773773006, 10155006, 1197589000, 720601000, 203645000, and 28 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q67.5?
Q67.5 is linked to 3 UMLS Concept Unique Identifiers: C0265675, C0158775, C0559260. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q67.5 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital deformity of spine 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 Q67.5?
Q67.5 maps to the ICD-11 code: LB73.Z (Structural developmental anomalies of spine or bony thorax, unspecified).
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.