Q07.8

Billable

Other specified congenital malformations of nervous system

Status

Billable / Specific

Chapter

17: Congenital Malformations, Deformations and Chromosomal Abnormalities

Parent Code

Q07

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

Agenesis of nerve
Displacement of brachial plexus
Jaw-winking syndrome
Marcus Gunn's syndrome

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(2)

Q07.0

Arnold-Chiari syndrome

Q07.9

Congenital malformation of nervous system, unspecified

Billable

ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

LA0ZStructural developmental anomalies of the nervous system, unspecifiedequivalentPrimary

Also Known As / Clinical Terms(319)

SNOMED CT

UMLS

Clinical Terms

Congenital hypoplasia of macula lutea
Brachial plexus displacement
Elejalde disease
PVH - Periventricular heterotopia
Congenital hypomyelinating neuropathy
Peripheral amyelination
Congenital achiasma
Disorder of optic tract
Ectopic neural glial masses
Congenital hypoplasia of vestibular nerve
Congenital adhesions of brain meninges
Congenital anomaly of membranous labyrinth
Deafness, encephaloneuropathy, obesity, valvulopathy syndrome
Abnormal innervation syndrome of eyelid
Congenital hypoplasia of optic tract
marcus gunn syndrome
Developmental displacement of brachial plexus
Hearing loss, encephaloneuropathy, obesity, valvulopathy syndrome
Portwine naevus
Marcus Gunn phenonemon
Mitochondrial deoxyribonucleic acid depletion syndrome, encephalomyopathic form with variable craniofacial anomalies
Schisis association syndrome
Ectopic glial tissue
Marcus-Gunn syndrome
Nova syndrome
winking jaw
Indifference to pain
Congenital indifference to pain
Congenital absence of myelination of peripheral nerve
FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome
Finding of pain tolerance
Cerebro-oculo-facio-skeletal syndrome
Port-wine stain of skin
Mitochondrial DNA depletion syndrome encephalomyopathic form
Congenital macular hypoplasia
Congenital deficiency of cochlear nerve
FBXL4-related early onset mitochondrial encephalopathy
Neuronal heterotopia
FHONDA syndrome
Congenital anomaly of cochlea
Port-wine naevi, mega cisterna magna, hydrocephalus syndrome
Naevus flammeus
Congenital retinal hypoplasia
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies
Congenital anomaly of macula
Meningeal adhesions
Congenital degeneration of nervous system
Oligophrenic cerebellolenticular degeneration
Marcus Gunn jaw winking synkinesis
Neuroectodermal melanolysosomal disease
Port-wine nevus
Cerebral meningeal adhesions
Marcus Gunn jaw-winking syndrome
Neuronal choristoma
Nerve agenesis
Jaw-winking syndrome (disorder)
Aplasia of optic nerve
Congenital ischaemic atrophy of central nervous system structure
jaw winking
Congenital hypoplasia of retina
Port-wine naevus
Congenital anomaly of the meninges
jaw-winking
Immature ganglionosis of large intestine
PLOSL - polycystic lipomembranous osteodysplasia with sclerosing leucoencephalopathy
Port-wine nevi, mega cisterna magna, hydrocephalus syndrome
Observation of pain tolerance
Port wine stain of skin
Marcus Gunn phenomenon
Congenital absence of optic chiasma
Mitochondrial DNA depletion syndrome 8A encephalomyopathic type with renal tubulopathy
Congenital hypoplasia of fovea
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
Hydranencephaly
Congenital absence of parasympathetic ganglion cells
Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
maxillopalpebral synkinesis
CAMAK - Cerebro-oculo-facio-skeletal syndrome
Congenital malformation of the meninges
Portwine nevus
Pena-Shokeir syndrome type 2
Congenital hypoplasia of corticospinal tract
Lyon's hypomyelinating neuropathy
PLOSL - polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
Congenital adhesions of cerebral meninges
Cataract, congenital heart disease, neural tube defect syndrome
Jaw-winking syndrome
Asymbolia
Disorder of neuronal migration and differentiation
Marcus-Gunn jaw winking
Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form
Congenital disorder of facial nerve
Congenital ischemic atrophy of central nervous system structure
PWS - Port-wine stain
CAMFAK - Cerebro-oculo-facio-skeletal syndrome
F-box and leucine rich repeat protein 4 related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form
Agenesis of nerve
Cochlear nerve disorder
Marcus-Gunn jaw-wink syndrome
Optic tract disorder
Cerebro-oculo-nasal syndrome
FHONDA (foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis) syndrome
Ribonucleotide reductase regulatory TP53 inducible subunit M2B-related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with renal tubulopathy
Isolated aplasia of optic nerve
Congenital anomaly of visual system
Presenile dementia with bone cysts
X-linked periventricular heterotopia
Pterygoid-levator synkinesis
Abnormal eyelid innervation syndrome
Congenital hypoplasia of olfactory tract
FBXL4 (F-box and leucine rich repeat protein 4) related early onset mitochondrial encephalopathy
Abnormality of neurogenesis
Congenital neurological degeneration
Adhesion of brain meninges
jaw wink
Congenital absence of cerebral hemispheres
Isolated optic nerve aplasia
Hemispheric cerebral hypoplasia
Marinesco-Sjögren syndrome
Cerebrooculonasal syndrome
Cochlear nerve deficiency
Brachial plexus displacement (disorder)
Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, hydranencephaly syndrome
mtDNA (mitochondrial deoxyribonucleic acid) depletion syndrome, encephalomyopathic form with variable craniofacial anomalies
Mitochondrial DNA depletion syndrome 13 encephalomyopathic type
Marinesco-Sjogren syndrome
Congenital hypoplasia of fovea centralis
Nasu-Hakola disease
Port-wine stain
Agenesis of nerve (disorder)
Aganglionosis of parasympathetic nerve ganglia
Schisis association
RRM2B-related mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
Polycystic lipomembranous osteodysplasia with sclerosing leucoencephalopathy
Marcus Gunn's syndrome
Congenital anomaly of the membranous labyrinth
Mega cisterna magna
COFS - Cerebro-oculo-facio-skeletal syndrome
Congenital hypoplasia of cerebral hemisphere
MARCH syndrome
jaw winking syndrome
COFS syndrome
Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome
Adhesion of meninges
Congenital anomaly of optic nerve
Optic nerve aplasia
Nevus flammeus
Congenital spastic foot
Spastic foot
Port-wine birthmark
Marcus Gunn jaw winking
familial Marcus Gunn phenomenon
Displacement of brachial plexus
Congenital pain asymbolia
Trigemino-oculomotor synkinesis

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.

How does Q07.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified congenital malformations of nervous system 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 Q07.8?

Q07.8 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.