G93.44
BillableAdult-onset leukodystrophy with axonal spheroids
Adult-onset leukodystrophy with axonal spheroids
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
Excludes 2
Conditions not included here, but the patient may have both
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •alcoholic encephalopathyG31.2
- •encephalopathy in diseases classified elsewhereG94
- •hypertensive encephalopathyI67.4
- •toxic (metabolic) encephalopathyG92.8
Related Codes(6)
G93.40Encephalopathy, unspecified
G93.41Metabolic encephalopathy
G93.42Megalencephalic leukoencephalopathy with subcortical cysts
G93.43Leukoencephalopathy with calcifications and cysts
G93.45Developmental and epileptic encephalopathy
G93.49Other encephalopathy
Also Known As / Clinical Terms(59)
UMLS
- ALSPC3711381
- Adult-Onset Leukodystrophy with Neuroaxonal SpheroidsC3711381
- Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented GliaC3711381
- Adult-onset leucodystrophy with neuroaxonal spheroidsC3711381
- Adult-onset leukodystrophy with axonal spheroidsC3711381
- Adult-onset leukodystrophy with neuroaxonal spheroidsC3711381
- Adult-onset leukoencephalopathy with axonal spheroids and pigmented gliaC3711381
- Autosomal Dominant Leukoencephalopathy with Neuroaxonal SpheroidsC3711381
- DEMENTIA, FAMILIAL, NEUMANN TYPEC3711381
- Dementia, Familial, Neumann TypeC3711381
- GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICALC3711381
- GPSCC3711381
- Gliosis, Familial Progressive SubcorticalC3711381
- HDLSC3711381
- HDLS - hereditary diffuse leucoencephalopathy with spheroidsC3711381
- HDLS - hereditary diffuse leukoencephalopathy with spheroidsC3711381
- Hereditary Diffuse Leukoencephalopathy with Axonal SpheroidsC3711381
- Hereditary Diffuse Leukoencephalopathy with SpheroidsC3711381
- Hereditary diffuse leucoencephalopathy with axonal spheroidsC3711381
- Hereditary diffuse leucoencephalopathy with spheroidsC3711381
- Hereditary diffuse leukoencephalopathy with axonal spheroidsC3711381
- Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented gliaC3711381
- Hereditary diffuse leukoencephalopathy with spheroidsC3711381
- Hereditary diffuse leukoencephalopathy with spheroids (disorder)C3711381
- LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANTC3711381
- LEUKOENCEPHALOPATHY, ADULT-ONSET, WITH AXONAL SPHEROIDS AND PIGMENTED GLIAC3711381
- LEUKOENCEPHALOPATHY, HEREDITARY DIFFUSE, WITH SPHEROIDSC3711381
- Leukoencephalopathy with Neuroaxonal Spheroids, Autosomal DominantC3711381
- Leukoencephalopathy, Diffuse Hereditary, With SpheroidsC3711381
- Neuroaxonal LeukodystrophyC3711381
- POLDC3711381
- Pigmentary Orthochromatic LeukodystrophyC3711381
- SUBCORTICAL GLIOSIS OF NEUMANNC3711381
- Subcortical Gliosis of NeumannC3711381
Clinical Terms
- Hereditary diffuse leucoencephalopathy with spheroids
- Leukoencephalopathy with Neuroaxonal Spheroids, Autosomal Dominant
- ALSP
- Adult-onset leukodystrophy with neuroaxonal spheroids
- HDLS
- Autosomal Dominant Leukoencephalopathy with Neuroaxonal Spheroids
- Hereditary diffuse leucoencephalopathy with axonal spheroids
- Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia
- Subcortical Gliosis of Neumann
- GPSC
- Hereditary diffuse leukoencephalopathy with axonal spheroids
- Gliosis, Familial Progressive Subcortical
- Hereditary Diffuse Leukoencephalopathy with Spheroids
- LEUKOENCEPHALOPATHY, ADULT-ONSET, WITH AXONAL SPHEROIDS AND PIGMENTED GLIA
- Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
- DEMENTIA, FAMILIAL, NEUMANN TYPE
- LEUKOENCEPHALOPATHY, HEREDITARY DIFFUSE, WITH SPHEROIDS
- Hereditary diffuse leukoencephalopathy with spheroids (disorder)
- POLD
- Neuroaxonal Leukodystrophy
- Adult-onset leucodystrophy with neuroaxonal spheroids
- HDLS - hereditary diffuse leukoencephalopathy with spheroids
- Pigmentary Orthochromatic Leukodystrophy
- HDLS - hereditary diffuse leucoencephalopathy with spheroids
- Leukoencephalopathy, Diffuse Hereditary, With Spheroids
Frequently Asked Questions
What is the ICD-10 code for adult-onset leukodystrophy with axonal spheroids?
The ICD-10-CM code for adult-onset leukodystrophy with axonal spheroids is G93.44. The full clinical description is "Adult-onset leukodystrophy with axonal spheroids". G93.44 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G93.44 mean?
ICD-10-CM code G93.44 represents “Adult-onset leukodystrophy with axonal spheroids”. 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 G93.44 a billable code?
Yes, G93.44 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G93.44 in?
G93.44 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What are the UMLS CUIs for G93.44?
G93.44 is linked to 1 UMLS Concept Unique Identifier: C3711381. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G93.44 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like adult-onset leukodystrophy with axonal spheroids 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 G93.44?
There is no direct ICD-11 mapping available for G93.44 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.
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.