Q06.8
BillableOther specified congenital malformations of spinal cord
Other specified congenital malformations of spinal cord
Coding Notes
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(6)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(85)
SNOMED CT
- Caudal dysplasia sequence8301004
- Caudal regression syndrome8301004
- Congenital dermal sinus70499005
- Congenital tethering of spinal cord70534000
- Occult spinal dysraphism sequence70534000
- Tethered cord malformation sequence70534000
- Tethered cord syndrome70534000
- Hemimyelia73331006
- Enterogenous cyst204766008
- Congenital absence of sacrum205425003
- Sacral agenesis205425003
- Abnormality of canalisation and retrogressive differentiation253188000
- Abnormality of canalization and retrogressive differentiation253188000
- Sacral dysgenesis253189008
- Lumbosacral agenesis253190004
- Myeloschisis360530005
- Primary tethered cord syndrome768939009
- Primary tethered spinal cord syndrome768939009
- Holoprosencephaly with caudal dysgenesis syndrome771146007
- Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome774150004
- Neurenteric cyst789120001
- Lipoma due to neurospinal dysraphism1003434002
- Neurenteric cyst of spine1144247000
- Neuroenteric cyst of spine1144247000
- Spinal neurenteric cyst1144247000
- Spinal neuroenteric cyst1144247000
- Dysraphism, cleft lip and palate, limb reduction defect syndrome1208338004
- Medeira Dennis Donnai syndrome1208338004
- Congenital spinal dermal sinus1303909005
- Dermal sinus tract1303909005
- Congenital retained medullary spinal cord1303912008
- Retained medullary cord1303912008
- Flat LDM (limited dorsal myeloschisis)1303914009
- Non-saccular LDM (limited dorsal myeloschisis)1303914009
- Non-saccular limited dorsal myeloschisis1303914009
- LDM - limited dorsal myeloschisis1303915005
- Limited dorsal myeloschisis1303915005
- Saccular LDM (limited dorsal myeloschisis)1303916006
- Saccular limited dorsal myeloschisis1303916006
- Dysraphism of cervical spine200021000119109
- Spinal dysraphism249491000119100
- Structural developmental anomalies of neurenteric canal249491000119100
Clinical Terms
- Sacral agenesis
- Congenital dermal sinus
- Saccular limited dorsal myeloschisis
- Dysraphism, cleft lip and palate, limb reduction defect syndrome
- Primary tethered cord syndrome
- Neurenteric cyst
- Holoprosencephaly with caudal dysgenesis syndrome
- Abnormality of canalisation and retrogressive differentiation
- Congenital retained medullary spinal cord
- Neuroenteric cyst of spine
- Lipoma due to neurospinal dysraphism
- Congenital spinal dermal sinus
- Limited dorsal myeloschisis
- Non-saccular LDM (limited dorsal myeloschisis)
- Non-saccular limited dorsal myeloschisis
- Abnormality of canalization and retrogressive differentiation
- Primary tethered spinal cord syndrome
- Retained medullary cord
- Congenital absence of sacrum
- Structural developmental anomalies of neurenteric canal
- Saccular LDM (limited dorsal myeloschisis)
- Enterogenous cyst
- Medeira Dennis Donnai syndrome
- Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome
- Neurenteric cyst of spine
- Spinal neurenteric cyst
- Dermal sinus tract
- Caudal regression syndrome
- Tethered cord malformation sequence
- Myeloschisis
- Occult spinal dysraphism sequence
- LDM - limited dorsal myeloschisis
- Dysraphism of cervical spine
- Lumbosacral agenesis
- Caudal dysplasia sequence
- Spinal dysraphism
- Spinal neuroenteric cyst
- Congenital tethering of spinal cord
- Hemimyelia
- Sacral dysgenesis
- Tethered cord syndrome
- Flat LDM (limited dorsal myeloschisis)
Frequently Asked Questions
What is the ICD-10 code for other specified congenital malformations of spinal cord?
The ICD-10-CM code for other specified congenital malformations of spinal cord is Q06.8. The full clinical description is "Other specified congenital malformations of spinal cord". Q06.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q06.8 mean?
ICD-10-CM code Q06.8 represents “Other specified congenital malformations of spinal cord”. 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 Q06.8 a billable code?
Yes, Q06.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q06.8 in?
Q06.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q06.8 map to?
Q06.8 maps to 24 SNOMED CT concepts: 253188000, 8301004, 205425003, 70499005, 1303912008, and 19 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q06.8?
Q06.8 is linked to 1 UMLS Concept Unique Identifier: C0477975. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q06.8 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified congenital malformations of spinal cord 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 Q06.8?
Q06.8 maps to the ICD-11 code: LA07.Z (Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column, 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.