Diagnosis Code: G31.89

Short Description: Other specified degenerative diseases of nervous system

Long Description: Other specified degenerative diseases of nervous system

The code G31.89 is VALID for claim submission

Code Classification:

• Diseases of the nervous system (G00–G99)
  • Other degenerative diseases of the nervous system (G30-G32)
    • Oth degenerative diseases of nervous system, NEC (G31)
      • G31.89 Other specified degenerative diseases of nervous system

Code Version: 2022 ICD-10-CM

Synonyms

• 3-Methylglutaconic aciduria type 4
• 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome
• Acute cerebellar syndrome
• Argyrophilic grain disease
• Arteriopathic granular atrophy of cerebral cortex
• Autoimmune cerebellar degeneration
• Autosomal dominant striatal neurodegeneration
• Autosomal recessive cerebral atrophy
• Axonal neuropathy
• Beta-propeller protein-associated neurodegeneration
• Cerebellar ataxia associated with another disorder
• Cerebellar deficiency syndrome
• Cerebral degeneration in childhood
• Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder
• Chorea co-occurrent and due to dentatorubropallidoluysian degeneration
• Chorea co-occurrent and due to Huntington disease-like condition
• Chorea co-occurrent and due to Huntington disease-like condition
• Chorea co-occurrent and due to Huntington disease-like condition
• Chorea due to chronic hepatocerebral degeneration
• Chorea due to hereditary ataxia
• Chorea due to heredodegenerative disorder
• Chorea due to heredodegenerative disorder
• Chorea due to Huntington disease-like 1
• Chorea due to Huntington disease-like 2
• Chorea due to Huntington disease-like 3
• Chronic hepatocerebral degeneration
• Coenzyme A synthase protein associated neurodegeneration
• Congenital cerebellar cortical atrophy
• Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome
• Corneal cerebellar syndrome
• Corticostriatal-spinal degeneration
• Cystic degeneration of brain
• Dentatorubropallidoluysian degeneration
• Dentatorubropallidoluysian degeneration
• Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome
• Disorder of valine metabolism
• Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome
• Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome
• Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome
• Fatal post-viral neurodegenerative disorder
• Fatty acid hydroxylase associated neurodegeneration
• Generalized dystonia
• Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome
• Hereditary acantholytic dermatosis
• Hereditary cerebellar atrophy
• Hereditary cerebellar atrophy
• Hereditary cerebellar atrophy
• Hereditary cerebellar atrophy
• Hereditary cerebellar atrophy
• Hereditary cerebellar atrophy
• Hereditary degenerative disease of central nervous system
• Huntington disease-like 1
• Huntington disease-like 3
• Huntington disease-like syndrome
• Huntington disease-like syndrome
• Huntington disease-like syndrome
• Huntington disease-like syndrome
• Huntington disease-like syndrome due to C9ORF72 expansions
• Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum
• Inborn error of amino acid metabolism
• Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
• Infantile neuroaxonal dystrophy
• Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome
• Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome
• Juvenile cerebellar degeneration AND myoclonus
• Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome
• Keratosis follicularis, dwarfism, cerebral atrophy syndrome
• Kufor Rakeb syndrome
• Late cortical cerebellar atrophy
• Late infantile and juvenile neuroaxonal dystrophy
• MEPAN syndrome
• Mitochondrial membrane protein associated neurodegeneration
• NADHX dehydratase deficiency
• NADHX epimerase deficiency
• Neuroaxonal dystrophy
• Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency
• Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome
• Olivopontocerebellar atrophy and deafness
• Olivopontocerebellar degeneration
• PCNA-related progressive neurodegenerative photosensitivity syndrome
• Pineal degeneration
• PRKAR1B-related neurodegenerative dementia with intermediate filaments
• Progressive cerebello-cerebral atrophy
• Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome
• Progressive neuronal degeneration of childhood
• Progressive neuronal degeneration without liver cirrhosis
• Second cranial nerve finding
• Severe neurodegenerative syndrome with lipodystrophy
• Sporadic cerebellar degeneration
• Synucleinopathy
• TUBB4A-related leukodystrophy
• USP18 deficiency
• X-linked neurodegenerative syndrome Bertini type
• X-linked neurodegenerative syndrome Hamel type

Crosswalk Information

Similar Codes

This page was last updated on: 10/1/2023

« Previous Code