Q07.8
BillableOther specified congenital malformations of nervous system
Other specified congenital malformations of nervous system
Status
Billable / Specific
Parent Code
Q07Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Agenesis of nerve
- Displacement of brachial plexus
- Jaw-winking syndrome
- Marcus Gunn's syndrome
Also Known As / Clinical Terms
SNOMED CT
- Congenital anomaly of macula4041005
- Indifference to pain16831006
- Congenital absence of cerebral hemispheres30023002
- Hydranencephaly30023002
- Congenital ischaemic atrophy of central nervous system structure31076000
- Congenital ischemic atrophy of central nervous system structure31076000
- Cochlear nerve disorder35141006
- CAMAK - Cerebro-oculo-facio-skeletal syndrome41283003
- CAMFAK - Cerebro-oculo-facio-skeletal syndrome41283003
- COFS - Cerebro-oculo-facio-skeletal syndrome41283003
- COFS syndrome41283003
- Cerebro-oculo-facio-skeletal syndrome41283003
- Pena-Shokeir syndrome type 241283003
- Ectopic glial tissue43427008
- Ectopic neural glial masses43427008
- Developmental displacement of brachial plexus46829007
- Aganglionosis of parasympathetic nerve ganglia64370005
- Congenital absence of parasympathetic ganglion cells64370005
- Congenital anomaly of membranous labyrinth67985002
- Congenital anomaly of the membranous labyrinth67985002
- Marinesco-Sjogren syndrome80734006
- Marinesco-Sjögren syndrome80734006
- Oligophrenic cerebellolenticular degeneration80734006
- Congenital degeneration of nervous system95477007
- Congenital neurological degeneration95477007
- Congenital anomaly of optic nerve95502000
- Disorder of optic tract95776004
- Optic tract disorder95776004
- Agenesis of nerve111338006
- Nerve agenesis111338006
- Congenital anomaly of visual system127329003
- Adhesion of brain meninges193071004
- Cerebral meningeal adhesions193071004
- Congenital adhesions of brain meninges204072001
- Congenital adhesions of cerebral meninges204072001
- Brachial plexus displacement204086002
- Congenital disorder of facial nerve230541001
- Congenital hypomyelinating neuropathy230562000
- Lyon's hypomyelinating neuropathy230562000
- Congenital spastic foot230779009
- Neuronal choristoma230794008
- Abnormality of neurogenesis253128003
- Disorder of neuronal migration and differentiation253146009
- Neuronal heterotopia253150002
- Congenital anomaly of the meninges253199003
- Congenital malformation of the meninges253199003
- Finding of pain tolerance299953003
- Observation of pain tolerance299953003
- Spastic foot307324001
- Asymbolia403605007
- Congenital indifference to pain403605007
- Congenital pain asymbolia403605007
- Naevus flammeus416377005
- Nevus flammeus416377005
- PWS - Port-wine stain416377005
- Port wine stain of skin416377005
- Port-wine birthmark416377005
- Port-wine naevus416377005
- Port-wine nevus416377005
- Port-wine stain416377005
- Port-wine stain of skin416377005
- Portwine naevus416377005
- Portwine nevus416377005
- Congenital hypoplasia of fovea429449002
- Congenital hypoplasia of fovea centralis429449002
- Mega cisterna magna447739003
- PVH - Periventricular heterotopia448227009
- X-linked periventricular heterotopia448227009
- Nasu-Hakola disease702347001
- PLOSL - polycystic lipomembranous osteodysplasia with sclerosing leucoencephalopathy702347001
- PLOSL - polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy702347001
- Polycystic lipomembranous osteodysplasia with sclerosing leucoencephalopathy702347001
- Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy702347001
- Presenile dementia with bone cysts702347001
- Schisis association718095000
- Schisis association syndrome718095000
- Cerebro-oculo-nasal syndrome720855003
- Cerebrooculonasal syndrome720855003
- Immature ganglionosis of large intestine722853000
- Aplasia of optic nerve722989007
- Optic nerve aplasia722989007
- Elejalde disease724091002
- Neuroectodermal melanolysosomal disease724091002
- Cataract, congenital heart disease, neural tube defect syndrome726704006
- Congenital absence of optic chiasma734031008
- Congenital achiasma734031008
- Deafness, encephaloneuropathy, obesity, valvulopathy syndrome763688008
- Hearing loss, encephaloneuropathy, obesity, valvulopathy syndrome763688008
- Mitochondrial DNA depletion syndrome 8A encephalomyopathic type with renal tubulopathy765100000
- Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy765100000
- RRM2B-related mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy765100000
- Ribonucleotide reductase regulatory TP53 inducible subunit M2B-related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with renal tubulopathy765100000
- Mitochondrial DNA depletion syndrome encephalomyopathic form765401006
- Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form765401006
- F-box and leucine rich repeat protein 4 related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form765403009
- FBXL4 (F-box and leucine rich repeat protein 4) related early onset mitochondrial encephalopathy765403009
- FBXL4-related early onset mitochondrial encephalopathy765403009
- FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome765403009
- Mitochondrial DNA depletion syndrome 13 encephalomyopathic type765403009
- FHONDA (foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis) syndrome782754006
- FHONDA syndrome782754006
- Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome782754006
- Nova syndrome783701002
- Port-wine naevi, mega cisterna magna, hydrocephalus syndrome783701002
- Port-wine nevi, mega cisterna magna, hydrocephalus syndrome783701002
- Congenital anomaly of cochlea897539005
- Congenital hypoplasia of cerebral hemisphere1144337000
- Hemispheric cerebral hypoplasia1144337000
- Congenital hypoplasia of olfactory tract1144388002
- Congenital hypoplasia of vestibular nerve1144396007
- Congenital hypoplasia of retina1144397003
- Congenital retinal hypoplasia1144397003
- Congenital hypoplasia of optic tract1144402004
- Congenital hypoplasia of macula lutea1144408000
- Congenital macular hypoplasia1144408000
- Congenital absence of myelination of peripheral nerve1144624009
- Peripheral amyelination1144624009
- MARCH syndrome1169358003
- Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, hydranencephaly syndrome1169358003
- Cochlear nerve deficiency1186656004
- Congenital deficiency of cochlear nerve1186656004
- Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies1208937004
- Mitochondrial deoxyribonucleic acid depletion syndrome, encephalomyopathic form with variable craniofacial anomalies1208937004
- mtDNA (mitochondrial deoxyribonucleic acid) depletion syndrome, encephalomyopathic form with variable craniofacial anomalies1208937004
- Isolated aplasia of optic nerve1285319006
- Isolated optic nerve aplasia1285319006
- Congenital hypoplasia of corticospinal tract1362151001
- Adhesion of meninges290241000119109
- Meningeal adhesions290241000119109
UMLS
- Abnormal eyelid innervation syndromeC0266521
- Abnormal innervation syndrome of eyelidC0266521
- JAW-WINKINGC0266521
- Jaw winkingC0266521
- Jaw-winking syndromeC0266521
- Jaw-winking syndrome (disorder)C0266521
- MARCUS GUNN PHENOMENONC0266521
- MAXILLOPALPEBRAL SYNKINESISC0266521
- Marcus Gunn jaw winkingC0266521
- Marcus Gunn jaw winking synkinesisC0266521
- Marcus Gunn jaw-winking syndromeC0266521
- Marcus Gunn phenomenonC0266521
- Marcus Gunn phenonemonC0266521
- Marcus Gunn syndromeC0266521
- Marcus Gunn's syndromeC0266521
- Marcus-Gunn jaw winkingC0266521
- Marcus-Gunn jaw-wink syndromeC0266521
- Marcus-Gunn syndromeC0266521
- Pterygoid-levator synkinesisC0266521
- Trigemino-oculomotor synkinesisC0266521
- familial Marcus Gunn phenomenonC0266521
- jaw winkC0266521
- jaw winkingC0266521
- jaw winking syndromeC0266521
- jaw-winkingC0266521
- marcus gunn syndromeC0266521
- maxillopalpebral synkinesisC0266521
- winking jawC0266521
- Agenesis of nerveC0266518
- Agenesis of nerve (disorder)C0266518
- Nerve agenesisC0266518
- Brachial plexus displacementC0344495
- Brachial plexus displacement (disorder)C0344495
- Displacement of brachial plexusC0344495
- Other specified congenital malformations of nervous systemC0477976
Frequently Asked Questions
What is the ICD-10 code for other specified congenital malformations of nervous system?
The ICD-10-CM code for other specified congenital malformations of nervous system is Q07.8. The full clinical description is "Other specified congenital malformations of nervous system". Q07.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q07.8 mean?
ICD-10-CM code Q07.8 represents "Other specified congenital malformations of nervous system". 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 Q07.8 a billable code?
Yes, Q07.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q07.8 in?
Q07.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q07.8 map to?
Q07.8 maps to 62 SNOMED CT concepts: 253128003, 193071004, 290241000119109, 64370005, 111338006, and 57 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q07.8?
Q07.8 is linked to 4 UMLS Concept Unique Identifiers: C0266521, C0266518, C0344495, C0477976. 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.