Chronic disease	Disorder of nervous system
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Chronic nervous system disorder (disorder)
	Chronic nervous system disorder
	Chronic nervous system disease Chronic disorder of nervous system Chronic disease of nervous system
	chronische ziekte van zenuwstelsel
	chronische aandoening van zenuwstelsel chronische aandoening van systema nervosum

Id	128283000
Status	Defined

Finding site

Structure of nervous system

Clinical course

ICD-10 complex map reference set

Target	G96.9
Rule	TRUE
Advice	ALWAYS G96.9
Correlation	SNOMED CT source code to target map code correlation not specified

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2-methyl-3-hydroxybutyric aciduria

Abdominal cutaneous nerve entrapment syndrome

Acute relapsing multiple sclerosis

Alexander's disease

Amyotrophic lateral sclerosis type 12

Amyotrophic lateral sclerosis type 10

Amyotrophic lateral sclerosis type 3

Amyotrophic lateral sclerosis type 4

Amyotrophic lateral sclerosis type 6

Amyotrophic lateral sclerosis type 7

Amyotrophic lateral sclerosis type 8

Amyotrophic lateral sclerosis type 9

Autosomal dominant adult-onset proximal spinal muscular atrophy

Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation

Autosomal dominant Charcot-Marie-Tooth disease type 2O

Autosomal dominant Charcot-Marie-Tooth disease type 2Q

Autosomal recessive intermediate Charcot-Marie-Tooth disease type C

Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy

Autosomal recessive lower motor neuron disease with childhood onset

Benign monomelic amyotrophy1

Benign multirecurrent endothelioleukocytal meningitis

Charcot-Marie-Tooth disease type 2B5

Charcot-Marie-Tooth disease type 2P

Childhood-onset spasticity with hyperglycinemia

Chronic brain syndrome92

Chronic central serous chorioretinopathy1

Chronic fatigue syndrome

Chronic infectious disease of central nervous system5

Chronic inflammatory demyelinating polyradiculoneuropathy2

Chronic intracranial subdural hematoma

Chronic meningitis5

Chronic mixed headache syndrome

Chronic mixed headache syndrome

Chronic motor tic disorder4

Chronic nerve root disorder

Chronic non-traumatic intracranial subdural hemorrhage

Chronic painful neuropathy due to diabetes mellitus1

Chronic painful polyneuropathy following chemotherapy

Chronic paralysis due to lesion of spinal cord2

Chronic paraplegia1

Chronic progressive paraparesis

Chronic relapsing inflammatory optic neuropathy

Chronic subdural hygroma

Chronic trochlear nerve palsy1

Chronic venous infarction of spinal cord

Complex regional pain syndrome5

Congenital cataract with ataxia and deafness syndrome

Demyelination of central nervous system co-occurrent and due to Behcet disease

Distal hereditary motor neuropathy type 1

Distal hereditary motor neuropathy type 2

Distal hereditary motor neuropathy type 7

Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome

Hereditary cerebral hemorrhage with amyloidosis2

Hereditary motor and sensory neuropathy type 5

Hereditary motor and sensory neuropathy with acrodystrophy

Idiopathic recurrent stupor

Intermittent horizontal conjugate gaze deviation

Intermittent upward gaze deviation

Juvenile amyotrophic lateral sclerosis2

Limb girdle muscular dystrophy due to POMK deficiency

Lower motor neuron syndrome with late-adult onset

Megaconial congenital muscular dystrophy

MME-related autosomal dominant Charcot Marie Tooth disease type 2

Multiple mitochondrial dysfunctions syndrome type 4

Muscle-eye-brain disease, congenital muscular dystrophy

Neuhauser Eichner Opitz syndrome

Neuronal ceroid lipofuscinosis 8

NKX6-2-related autosomal recessive hypomyelinating leukodystrophy

Non-recovering brachial plexus injury due to birth trauma

PCNA-related progressive neurodegenerative photosensitivity syndrome

Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome

Persistent idiopathic facial pain

Persistent neonatal myasthenia gravis

Progressive cone-rod dystrophy

Progressive external ophthalmoplegia9

Progressive multiple sclerosis3

Progressive muscular atrophy2

Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome

Pure autonomic failure1

Recurrent atlantoaxial subluxation with myelopathy

Recurrent carpal tunnel syndrome

Recurrent idiopathic neuroretinitis

Severe neurodegenerative syndrome with lipodystrophy

Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome

X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome

Young adult-onset distal hereditary motor neuropathy