G93.49
BillableOther encephalopathy
Other encephalopathy
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Encephalopathy NEC
Excludes 2
Conditions not included here, but the patient may have both
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- alcoholic encephalopathy (G31.2)
- encephalopathy in diseases classified elsewhere (G94)
- hypertensive encephalopathy (I67.4)
- toxic (metabolic) encephalopathy (G92.8)
Also Known As / Clinical Terms
SNOMED CT
- Cerebral degeneration in childhood2584003
- Delayed dentition5639000
- Delayed eruption of tooth5639000
- Delayed tooth eruption5639000
- Late tooth eruption5639000
- Macroencephaly9740002
- Megalencephaly9740002
- Leucoencephalopathy22811006
- Leukoencephalopathy22811006
- Infantile encephalopathy AND lactic acidosis76938004
- Duchenne-Aran muscular atrophy88923002
- PMA - Progressive muscular atrophy88923002
- Progressive muscular atrophy88923002
- Pure progressive muscular atrophy88923002
- Binswanger's dementia90099008
- Binswanger's disease90099008
- Binswanger's encephalopathy90099008
- Chronic progressive subcortical encephalopathy90099008
- Encephalitis subcorticalis chronica90099008
- Subcortical arteriosclerotic encephalopathy90099008
- Subcortical atherosclerotic dementia90099008
- Subcortical leucoencephalopathy90099008
- Subcortical leukoencephalopathy90099008
- Optic nerve finding106152006
- Second cranial nerve finding106152006
- Amino acid below reference range124057005
- Decreased amino acid124057005
- Cerebral degeneration due to cerebrovascular disease192813004
- HIV - Human immunodeficiency virus leucoencephalopathy230180003
- HIV - Human immunodeficiency virus leukoencephalopathy230180003
- Human immunodeficiency virus leucoencephalopathy230180003
- Human immunodeficiency virus leukoencephalopathy230180003
- Distal spinal muscular atrophy230247001
- Subcortical vascular dementia230286002
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy390936003
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy390936003
- Punctate palmoplantar keratoderma402773000
- Multifactorial encephalopathy423144007
- PEHO (progressive encephalopathy with edema, hypsarrhythmia and optic atrophy) syndrome442511009
- PEHO (progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy) syndrome442511009
- PEHO syndrome442511009
- Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome442511009
- Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy syndrome442511009
- Cerebral small vessel disease443929000
- Small vessel cerebrovascular disease443929000
- HCC - hypomyelination and congenital cataract702379005
- Hypomyelination and congenital cataract702379005
- Familial dementia with neuroserpin inclusion bodies702421006
- Familial encephalopathy with neuroserpin inclusion bodies702421006
- Adult-onset leucodystrophy with neuroaxonal spheroids702427005
- Adult-onset leukodystrophy with neuroaxonal spheroids702427005
- HDLS - hereditary diffuse leucoencephalopathy with spheroids702427005
- HDLS - hereditary diffuse leukoencephalopathy with spheroids702427005
- Hereditary diffuse leucoencephalopathy with axonal spheroids702427005
- Hereditary diffuse leucoencephalopathy with spheroids702427005
- Hereditary diffuse leukoencephalopathy with axonal spheroids702427005
- Hereditary diffuse leukoencephalopathy with spheroids702427005
- CARASIL syndrome703219008
- Cerebral autosomal recessive arteriopathy with subcortical infarcts and leucoencephalopathy703219008
- Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy703219008
- Maeda syndrome703219008
- Nemoto disease703219008
- Infantile leucoencephalopathy and megalencephaly703536004
- Infantile leukoencephalopathy and megalencephaly703536004
- Leucoencephalopathy with swelling and cysts703536004
- Leukoencephalopathy with swelling and cysts703536004
- Megalencephalic leucoencephalopathy with subcortical cysts703536004
- Megalencephalic leukoencephalopathy with subcortical cysts703536004
- Vacuolating leucoencephalopathy703536004
- Vacuolating leukoencephalopathy703536004
- Vacuolating megalencephalic leucoencephalopathy with subcortical cysts703536004
- Vacuolating megalencephalic leukoencephalopathy with subcortical cysts703536004
- Van der Knapp disease703536004
- Progressive cavitating leucoencephalopathy719267003
- Progressive cavitating leukoencephalopathy719267003
- Leucoencephalopathy co-occurrent with bilateral anterior temporal lobe cysts719403003
- Leukoencephalopathy co-occurrent with bilateral anterior temporal lobe cysts719403003
- Leucoencephalopathy with metaphyseal chondrodysplasia syndrome719405005
- Leukoencephalopathy with metaphyseal chondrodysplasia syndrome719405005
- Cystic leucoencephalopathy without megalencephaly720825005
- Cystic leukoencephalopathy without megalencephaly720825005
- White matter disorder caused by infection722601005
- White matter disorder co-occurrent and due to cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy724779000
- White matter disorder co-occurrent and due to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy724779000
- White matter disorder with CADASIL724779000
- Leucoencephalopathy, dystonia, motor neuropathy syndrome733452000
- Leukoencephalopathy, dystonia, motor neuropathy syndrome733452000
- Leucoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome735421004
- Leucoencephalopathy with brain stem and spinal cord involvement and lactate elevation syndrome735421004
- Leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome735421004
- Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation syndrome735421004
- Subcortical dementia762707000
- COXPD12 - combined oxidative phosphorylation defect type 12763366000
- Combined oxidative phosphorylation defect type 12763366000
- Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome763366000
- Ataxia, delayed dentition, hypomyelination syndrome764095005
- Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome764095005
- Anti-IgLON5 disease765751002
- Anti-IgLON5 syndrome765751002
- Autoimmune encephalopathy with parasomnia and obstructive sleep apnea765751002
- Autoimmune encephalopathy with parasomnia and obstructive sleep apnoea765751002
- Acute encephalopathy with biphasic seizures and late reduced diffusion766044005
- Acute infantile encephalopathy predominantly affecting frontal lobe766044005
- CLCN2 (chloride voltage-gated channel 2) related leucoencephalopathy768663003
- CLCN2 (chloride voltage-gated channel 2) related leukoencephalopathy768663003
- CLCN2-related leucoencephalopathy768663003
- CLCN2-related leukoencephalopathy768663003
- Leucoencephalopathy with ataxia768663003
- Leucoencephalopathy with mild cerebellar ataxia and white matter oedema768663003
- Leukoencephalopathy with ataxia768663003
- Leukoencephalopathy with mild cerebellar ataxia and white matter edema768663003
- STXBP1 developmental and epileptic encephalopathy768666006
- STXBP1-DEE - STXBP1 developmental and epileptic encephalopathy768666006
- Syntaxin binding protein 1 developmental and epileptic encephalopathy768666006
- Leucoencephalopathy, palmoplantar keratoderma syndrome771184001
- Leukoencephalopathy, palmoplantar keratoderma syndrome771184001
- Autosomal recessive leukoencephalopathy, ischaemic stroke, retinitis pigmentosa syndrome771476007
- Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome771476007
- SCN2A encephalopathy778002005
- Sodium voltage-gated channel alpha subunit 2 encephalopathy778002005
- COL4A1-related brain small vessel disease with haemorrhage778060000
- COL4A1-related brain small vessel disease with hemorrhage778060000
- COL4A1-related familial vascular leucoencephalopathy778060000
- COL4A1-related familial vascular leukoencephalopathy778060000
- COL4A1-related retinal arteriolar tortuosity, infantile hemiparesis, autosomal dominant leucoencephalopathy syndrome778060000
- COL4A1-related retinal arteriolar tortuosity, infantile hemiparesis, autosomal dominant leukoencephalopathy syndrome778060000
- Collagen type IV alpha 1 chain related familial vascular leucoencephalopathy778060000
- Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy778060000
- RVCL - retinal vasculopathy cerebral leucoencephalopathy783787000
- RVCL - retinal vasculopathy cerebral leukoencephalopathy783787000
- RVCL-S - retinal vasculopathy, cerebral leucoencephalopathy, systemic manifestations783787000
- RVCL-S - retinal vasculopathy, cerebral leukoencephalopathy, systemic manifestations783787000
- Retinal vasculopathy with cerebral leucoencephalopathy and systemic manifestations783787000
- Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations783787000
- ARSAL - autosomal recessive spastic ataxia with leucoencephalopathy784343003
- ARSAL - autosomal recessive spastic ataxia with leukoencephalopathy784343003
- Autosomal recessive spastic ataxia type 3784343003
- Autosomal recessive spastic ataxia with leucoencephalopathy784343003
- Autosomal recessive spastic ataxia with leukoencephalopathy784343003
- SPAX3 - autosomal recessive spastic ataxia type 3784343003
- Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome1169356004
- Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome1172588008
- Labrune syndrome1186710001
- Leucoencephalopathy with calcifications and cysts1186710001
- Leukoencephalopathy with calcifications and cysts1186710001
- Leucoencephalopathy due to copper deficiency1186819005
- Leucoencephalopathy due to hypocupremia1186819005
- Leukoencephalopathy due to copper deficiency1186819005
- Leukoencephalopathy due to hypocupremia1186819005
- 4H leucodystrophy1208933000
- 4H leukodystrophy1208933000
- POLR-related leucodystrophy1208933000
- POLR-related leukodystrophy1208933000
- Early-onset calcifying leucoencephalopathy, skeletal dysplasia1222661007
- Early-onset calcifying leukoencephalopathy, skeletal dysplasia1222661007
- PYCR2-related microcephaly, progressive leucoencephalopathy1237421000
- PYCR2-related microcephaly, progressive leukoencephalopathy1237421000
- Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leucoencephalopathy1237421000
- Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leukoencephalopathy1237421000
- Adult-onset progressive leucoencephalopathy, early-onset deafness1299152003
- Adult-onset progressive leucoencephalopathy, early-onset hearing loss1299152003
- Adult-onset progressive leukoencephalopathy, early-onset deafness1299152003
- Adult-onset progressive leukoencephalopathy, early-onset hearing loss1299152003
- Encephalopathy caused by ionising radiation1339025008
- Encephalopathy caused by ionizing radiation1339025008
- Developmental delay, immunodeficiency, leucoencephalopathy, hypohomocysteinemia syndrome1340174002
- Developmental delay, immunodeficiency, leukoencephalopathy, hypohomocysteinemia syndrome1340174002
- Encephalopathy caused by Influenza A virus10677711000119101
Frequently Asked Questions
What is the ICD-10 code for other encephalopathy?
The ICD-10-CM code for other encephalopathy is G93.49. The full clinical description is "Other encephalopathy". G93.49 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G93.49 mean?
ICD-10-CM code G93.49 represents "Other 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 G93.49 a billable code?
Yes, G93.49 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G93.49 in?
G93.49 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G93.49 map to?
G93.49 maps to 55 SNOMED CT concepts: 1208933000, 784343003, 766044005, 702427005, 1299152003, and 50 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G93.49?
G93.49 is linked to 1 UMLS Concept Unique Identifier: C1260408. 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.