Q07.9
BillableCongenital malformation of nervous system, unspecified
Congenital malformation of nervous system, unspecified
Status
Billable / Specific
Parent Code
Q07Coding 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
Also Known As / Clinical Terms
SNOMED CT
- Pili torti17170005
- Twisted hair17170005
- Congenital anomaly of the peripheral nervous system22133005
- Congenital anomaly of peripheral nerve23880008
- Congenital hepatic fibrosis79607001
- Congenital anomaly of nervous system88425004
- Congenital deformity of nervous system88425004
- Congenital disease of nervous system88425004
- Congenital lesion of nervous system88425004
- Congenital malformation of the nervous system88425004
- Cerebrofacial dysplasia109561000
- COD-MD - Cerebro-oculo-dysgenesis-muscular dystrophy syndrome111505001
- Cerebro-oculo-dysgenesis-muscular dystrophy syndrome111505001
- Muscle-eye-brain disease, congenital muscular dystrophy111505001
- Congenital anomaly of central nervous system128124001
- Congenital malformation of central nervous system128124001
- Congenital polyneuropathy230560008
- NTD - Neural tube defect253098009
- Neural tube defect253098009
- Vascular malformation of the nervous system253193002
- Congenital anomaly of the meninges253199003
- Congenital malformation of the meninges253199003
- Combined malformation of central nervous system and skeletal muscle277949001
- Muscle eye brain disease277950001
- Congenital anomaly of nervous system of head/neck287080001
- Congenital anomaly of neural structure of trunk363034005
- Immature autonomic stability371109001
- Immature autonomic system371109001
- Hypertrophic mitochondrial cardiomyopathy472316006
- Naevus sebaceous707136009
- Naevus sebaceous of Jadassohn707136009
- Nevus sebaceous707136009
- Nevus sebaceous of Jadassohn707136009
- Organoid naevus707136009
- Organoid nevus707136009
- Sebaceous naevus707136009
- Sebaceous nevus707136009
- Pili torti with developmental delay and neurological abnormality syndrome716194005
- Congenital cataract, nephropathy, encephalopathy syndrome722381004
- Crome syndrome722381004
- Congenital malformation of autonomic nervous system722996009
- Coenzyme Q10 deficiency724575009
- Freire Maia Pinheiro Opitz syndrome725908007
- NFDR (neurofaciodigitorenal) syndrome725908007
- Neurofaciodigitorenal syndrome725908007
- Cyprus facial neuromusculoskeletal syndrome732261005
- Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome734017008
- Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome763280005
- HIVEP2 (human immunodeficiency virus type I enhancer binding protein 2) related intellectual disability765434008
- HIVEP2-related intellectual disability765434008
- Human immunodeficiency virus type I enhancer binding protein 2 related intellectual disability765434008
- Goldston syndrome773737004
- Meckel syndrome type 7773737004
- Meckel-like syndrome type 1773737004
- NPHP3 (nephrocystin 3) related Meckel-like syndrome773737004
- NPHP3-related Meckel-like syndrome773737004
- Nephrocystin 3-related Meckel-like syndrome773737004
- Renal, hepatic, pancreatic dysplasia, Dandy-Walker cysts syndrome773737004
- FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome774070008
- Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome774070008
- SCALP syndrome774208009
- Sebaceous naevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented naevus syndrome774208009
- Sebaceous nevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented nevus syndrome774208009
- MEND (male emopamil-binding protein disorder with neurological defect) syndrome782739000
- Male EBP (emopamil-binding protein) disorder with neurological defect782739000
- Male emopamil-binding protein disorder with neurological defect782739000
- Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation784344009
- Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation784344009
- Navajo neurohepatopathy784346006
- Navajo neuropathy784346006
- Hypoplasia of optic nerve due to central nervous system malformation1003422005
- Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome1172630000
UMLS
- ABNORM NERVOUS SYSTEMC0497552
- Abnormalities, Congenital, Nervous SystemC0497552
- ABNORM CONGEN NERVOUS SYSTEMC0497552
- Abnormalities, Nervous SystemC0497552
- Abnormality of the nervous systemC0497552
- Abnormality, Nervous SystemC0497552
- Anomalies, Nervous SystemC0497552
- Anomaly, Nervous SystemC0497552
- CONGEN ABNORM NERVOUS SYSTEMC0497552
- CONGEN ANOMALIES NERVOUS SYSTEMC0497552
- CONGEN MALFORMATIONS NERVOUS SYSTEMC0497552
- Congenital Abnormalities, Nervous SystemC0497552
- Congenital Anomalies, Nervous SystemC0497552
- Congenital Malformations, Nervous SystemC0497552
- Congenital Nervous System DisorderC0497552
- Congenital anomaly NOS of nervous systemC0497552
- Congenital anomaly of nervous systemC0497552
- Congenital anomaly of nervous system (disorder)C0497552
- Congenital deformity NOS of nervous systemC0497552
- Congenital deformity of nervous systemC0497552
- Congenital disease of nervous systemC0497552
- Congenital lesion of nervous systemC0497552
- Congenital malformation of nervous system, unspecifiedC0497552
- Congenital malformation of the nervous systemC0497552
- Congenital malformations of the nervous system (Q00-Q07)C0497552
- MALFORMATIONS NERVOUS SYSTEM CONGENC0497552
- Malformation, Nervous SystemC0497552
- Malformations, Nervous SystemC0497552
- Malformations, Nervous System, CongenitalC0497552
- NERVOUS SYSTEM ABNORMC0497552
- NERVOUS SYSTEM CONGEN ABNORMC0497552
- NERVOUS SYSTEM CONGEN MALFORMATIONSC0497552
- NERVOUS SYSTEM MALFORMATIONS CONGENC0497552
- Nervous System AbnormalitiesC0497552
- Nervous System AbnormalityC0497552
- Nervous System AnomaliesC0497552
- Nervous System AnomalyC0497552
- Nervous System Congenital AbnormalitiesC0497552
- Nervous System Congenital MalformationsC0497552
- Nervous System MalformationC0497552
- Nervous System MalformationsC0497552
- Nervous System Malformations, CongenitalC0497552
- Neurologic abnormalitiesC0497552
- Neurological abnormalityC0497552
- congenital nervous system disorderC0497552
- Congenital disease or lesion NOS of nervous systemC2910110
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.
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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.