Q67.5
BillableCongenital deformity of spine
Congenital deformity of spine
Status
Billable / Specific
Parent Code
Q67Coding 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
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
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
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.
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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.