AutoICD API

G93.41

Billable

Metabolic encephalopathy

Metabolic encephalopathy

Status

Billable / Specific

Block

G89-G99

Parent Code

G93.4

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Septic encephalopathy

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(6)
G93.40

Encephalopathy, unspecified

BillableG93.42

Megalencephalic leukoencephalopathy with subcortical cysts

BillableG93.43

Leukoencephalopathy with calcifications and cysts

BillableG93.44

Adult-onset leukodystrophy with axonal spheroids

BillableG93.45

Developmental and epileptic encephalopathy

BillableG93.49

Other encephalopathy

Billable
Also Known As / Clinical Terms(252)

SNOMED CT

UMLS

Clinical Terms

  • METAB DIS BRAIN
  • Metabolic Brain Syndrome
  • Infantile non-ketotic hyperglycinaemia
  • metabolic brain diseases
  • Dialysis dysequilibrium syndrome
  • Mitochondrial encephalomyopathy
  • Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency
  • Brain Metabolic Disorders
  • Hyperglycinemia
  • Encephalopathy, Sepsis Associated
  • Mitochondrial myoencephalopathy
  • 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome
  • METAB BRAIN SYNDROMES
  • Sepsis Associated Encephalopathy
  • HD - Acute complications of haemodialysis
  • Mitochondrial neurogastrointestinal encephalomyopathy syndrome
  • Acute disorder of haemodialysis
  • Myxedema encephalopathy
  • Uraemic encephalopathy
  • Metabolic Brain Disease
  • Encephalopathy due to sulfite oxidase deficiency
  • Metabolic Brain Disorders
  • Sepsis-associated encephalopathy
  • Acute reversible leucoencephalopathy due to sodium-dependent dicarboxylate transporter deficiency
  • Non-ketotic hyperglycinaemia
  • 3-methylglutaconic aciduria with deafness, encephalopathy, Leigh-like syndrome
  • Brain Disorders, Metabolic
  • Metabolic encephalopathy NOS
  • Atypical non-ketotic hyperglycinaemia
  • Non ketotic hyperglycinaemia
  • Acute reversible leukoencephalopathy with increased urinary alpha-ketoglutarate
  • Thiamine-responsive encephalopathy
  • Complication of hemodialysis
  • BRAIN DIS METAB
  • NKH - Non-ketotic hyperglycinemia
  • Dialysis disequilibrium syndrome
  • 3-methylglutaconic aciduria with hearing loss, encephalopathy, Leigh-like syndrome
  • Brain Disease, Metabolic
  • Non-ketotic hyperglycinemia
  • Dialysis disequilibrium
  • Glucose transporter protein type 1 deficiency syndrome
  • Childhood encephalopathy due to thiamin pyrophosphokinase deficiency
  • Complication of haemodialysis
  • Transport and golgi organization 2 homolog-related metabolic encephalopathy, arrhythmia syndrome
  • Infantile non-ketotic hyperglycinemia
  • Sepsis-associated mental obtundation
  • Acute reversible leucoencephalopathy with increased urinary alpha-ketoglutarate
  • Infantile glycine encephalopathy
  • MEGDEL syndrome
  • Inborn error of amino acid metabolism
  • Non ketotic hyperglycinemia
  • Metabolic Disorder, Brain
  • Mitochondrial encephalomyopathy due to combined oxidative phosphorylation deficiency 6
  • Ethylmalonic encephalopathy protein 1 deficiency
  • Encephalopathy, Sepsis-Associated
  • Mitochondrial encephalomyopathy due to COXPD6 deficiency
  • Sepsis-Associated Encephalopathies
  • ENCEPH METAB
  • Associated Encephalopathy, Sepsis
  • METAB ENCEPH
  • Encephalopathy, Metabolic
  • Childhood encephalopathy due to thiamine pyrophosphokinase deficiency
  • Disorder of glycine cleavage enzyme complex
  • TANGO2-related metabolic encephalopathy, arrhythmia syndrome
  • TMEM70 related mitochondrial encephalo-cardio-myopathy
  • METAB BRAIN DIS
  • NKH - Non-ketotic hyperglycinaemia
  • Metabolic Encephalopathies
  • Martsolf-like syndrome
  • Septic encephalopathy
  • ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement
  • Encephalopathies, Sepsis-Associated
  • encephalopathy metabolic
  • Encephalopathies, Sepsis Associated
  • Encephalopathy due to sulphite oxidase deficiency
  • 3-Methylglutaconic aciduria type 4
  • Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement
  • Brain Diseases, Metabolic
  • Encephalopathy due to mitochondrial and peroxisomal fission defect
  • Deficiency of dioxygenase
  • Secondary amyloid encephalopathy
  • Myxoedema encephalopathy
  • DDS - dialysis disequilibrium syndrome
  • Brain Metabolic Disorder
  • Acute disorder of hemodialysis
  • Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome
  • Metabolic Brain Syndromes
  • Encephalopathy with sepsis
  • Urate encephalopathy
  • Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency
  • Acute reversible leukoencephalopathy due to sodium-dependent dicarboxylate transporter deficiency
  • Transport and golgi organisation 2 homolog-related metabolic encephalopathy, arrhythmia syndrome
  • Encephalopathy with sepsis (disorder)
  • BRAIN SYNDROME METAB
  • Metabolic encephalopathy (disorder)
  • Severe X-linked mitochondrial encephalomyopathy
  • Atypical non-ketotic hyperglycinemia
  • metabolic disorders brain
  • Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation
  • HD - Acute complications of hemodialysis
  • Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome
  • Ethylmalonic encephalopathy
  • Hyperaminoaciduria
  • Associated Encephalopathies, Sepsis
  • Brain Syndrome, Metabolic
  • Encephalopathies, Metabolic
  • Hyperglycinaemia
  • Metabolic Disorders, Brain
  • Metabolic Brain Disorder
  • Sepsis Associated Encephalopathies
  • Hyponatremic encephalopathy
  • Hyponatraemic encephalopathy
  • Uremic encephalopathy
  • Acute reversible leukoencephalopathy due to SLC13A3 deficiency
  • Acute reversible leucoencephalopathy due to SLC13A3 deficiency
  • Brain Disorder, Metabolic
  • Progressive polyneuropathy with bilateral striatal necrosis
  • METAB BRAIN SYNDROME
  • Asparagine synthetase deficiency
  • Atypical glycine encephalopathy
Frequently Asked Questions
What is the ICD-10 code for metabolic encephalopathy?

The ICD-10-CM code for metabolic encephalopathy is G93.41. The full clinical description is "Metabolic encephalopathy". G93.41 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code G93.41 mean?

ICD-10-CM code G93.41 represents “Metabolic encephalopathy”. It is classified under Chapter 6: Diseases of the Nervous System and is a billable/specific code that can be used on a claim.

Is G93.41 a billable code?

Yes, G93.41 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is G93.41 in?

G93.41 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).

What SNOMED CT codes does G93.41 map to?

G93.41 maps to 35 SNOMED CT concepts: 297233004, 711409002, 236538004, 1340040004, 782757004, and 30 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for G93.41?

G93.41 is linked to 2 UMLS Concept Unique Identifiers: C0393642, C0006112. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does G93.41 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like metabolic encephalopathy 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 G93.41?

There is no direct ICD-11 mapping available for G93.41 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

Automate ICD-10 Coding With AI

Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.

Try FreeView API Docs

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.