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Q07.9

Billable

Congenital malformation of nervous system, unspecified

Congenital malformation of nervous system, unspecified

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Congenital anomaly NOS of nervous system
  • Congenital deformity NOS of nervous system
  • Congenital disease or lesion NOS of nervous system
Related Codes(2)
ICD-11 Equivalents(1)

ICD-11 Equivalents

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Corresponding ICD-11 codes from the WHO crosswalk mapping

Also Known As / Clinical Terms(229)

SNOMED CT

UMLS

Clinical Terms

  • Sebaceous naevus
  • NERVOUS SYSTEM ABNORM
  • Congenital anomaly of central nervous system
  • Congenital malformation of central nervous system
  • Navajo neuropathy
  • Nervous System Malformations
  • Congenital Malformations, Nervous System
  • NERVOUS SYSTEM MALFORMATIONS CONGEN
  • SCALP syndrome
  • Coenzyme Q10 deficiency
  • Pili torti with developmental delay and neurological abnormality syndrome
  • Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
  • Neurofaciodigitorenal syndrome
  • Abnormalities, Nervous System
  • Sebaceous nevus
  • Renal, hepatic, pancreatic dysplasia, Dandy-Walker cysts syndrome
  • Crome syndrome
  • Congenital anomaly of peripheral nerve
  • Sebaceous nevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented nevus syndrome
  • CONGEN MALFORMATIONS NERVOUS SYSTEM
  • Congenital lesion of nervous system
  • Congenital polyneuropathy
  • Nervous System Anomalies
  • Male emopamil-binding protein disorder with neurological defect
  • Abnormality of the nervous system
  • Nevus sebaceous of Jadassohn
  • Congenital Anomalies, Nervous System
  • Cyprus facial neuromusculoskeletal syndrome
  • NERVOUS SYSTEM CONGEN ABNORM
  • Twisted hair
  • Navajo neurohepatopathy
  • Meckel syndrome type 7
  • Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation
  • Nervous System Malformation
  • Congenital cataract, nephropathy, encephalopathy syndrome
  • NTD - Neural tube defect
  • Hypertrophic mitochondrial cardiomyopathy
  • Congenital disease of nervous system
  • Congenital malformations of the nervous system (Q00-Q07)
  • Congenital malformation of the nervous system
  • Nervous System Congenital Abnormalities
  • Muscle-eye-brain disease, congenital muscular dystrophy
  • Congenital anomaly of the meninges
  • Sebaceous naevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented naevus syndrome
  • Congenital deformity of nervous system
  • Congenital deformity NOS of nervous system
  • Vascular malformation of the nervous system
  • Nervous System Abnormality
  • Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome
  • HIVEP2-related intellectual disability
  • Cerebro-oculo-dysgenesis-muscular dystrophy syndrome
  • NPHP3 (nephrocystin 3) related Meckel-like syndrome
  • Congenital malformation of the meninges
  • Human immunodeficiency virus type I enhancer binding protein 2 related intellectual disability
  • Naevus sebaceous
  • Malformations, Nervous System
  • CONGEN ABNORM NERVOUS SYSTEM
  • ABNORM NERVOUS SYSTEM
  • Nervous System Abnormalities
  • Congenital anomaly of nervous system
  • Neural tube defect
  • NERVOUS SYSTEM CONGEN MALFORMATIONS
  • ABNORM CONGEN NERVOUS SYSTEM
  • Anomaly, Nervous System
  • COD-MD - Cerebro-oculo-dysgenesis-muscular dystrophy syndrome
  • NPHP3-related Meckel-like syndrome
  • Immature autonomic system
  • Nephrocystin 3-related Meckel-like syndrome
  • Congenital malformation of autonomic nervous system
  • Combined malformation of central nervous system and skeletal muscle
  • Congenital anomaly of the peripheral nervous system
  • Anomalies, Nervous System
  • Nevus sebaceous
  • Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome
  • Abnormality, Nervous System
  • Congenital Nervous System Disorder
  • Malformation, Nervous System
  • Congenital anomaly of nervous system of head/neck
  • Congenital disease or lesion NOS of nervous system
  • Immature autonomic stability
  • Nervous System Malformations, Congenital
  • Abnormalities, Congenital, Nervous System
  • Nervous System Congenital Malformations
  • Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome
  • Organoid nevus
  • CONGEN ANOMALIES NERVOUS SYSTEM
  • Cerebrofacial dysplasia
  • FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome
  • Male EBP (emopamil-binding protein) disorder with neurological defect
  • Congenital Abnormalities, Nervous System
  • Congenital anomaly of nervous system (disorder)
  • Goldston syndrome
  • Naevus sebaceous of Jadassohn
  • Hypoplasia of optic nerve due to central nervous system malformation
  • Meckel-like syndrome type 1
  • Congenital anomaly NOS of nervous system
  • Freire Maia Pinheiro Opitz syndrome
  • Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome
  • Neurologic abnormalities
  • HIVEP2 (human immunodeficiency virus type I enhancer binding protein 2) related intellectual disability
  • NFDR (neurofaciodigitorenal) syndrome
  • MALFORMATIONS NERVOUS SYSTEM CONGEN
  • MEND (male emopamil-binding protein disorder with neurological defect) syndrome
  • Congenital anomaly of neural structure of trunk
  • Organoid naevus
  • Neurological abnormality
  • Nervous System Anomaly
  • Muscle eye brain disease
  • Congenital hepatic fibrosis
  • Malformations, Nervous System, Congenital
  • Pili torti
Frequently Asked Questions
What is the ICD-10 code for congenital malformation of nervous system, unspecified?

The ICD-10-CM code for congenital malformation of nervous system, unspecified is Q07.9. The full clinical description is "Congenital malformation of nervous system, unspecified". Q07.9 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q07.9 mean?

ICD-10-CM code Q07.9 represents “Congenital malformation of nervous system, 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 Q07.9 a billable code?

Yes, Q07.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q07.9 in?

Q07.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q07.9 map to?

Q07.9 maps to 36 SNOMED CT concepts: 111505001, 109561000, 724575009, 277949001, 128124001, and 31 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q07.9?

Q07.9 is linked to 2 UMLS Concept Unique Identifiers: C0497552, C2910110. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q07.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformation of nervous system, 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 Q07.9?

Q07.9 maps to the ICD-11 code: LA0Z (Structural developmental anomalies of the nervous system, 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.