E75.25
BillableMetachromatic leukodystrophy
Metachromatic leukodystrophy
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •transitory endocrine and metabolic disorders specific to newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- •mucolipidosis, types I-IIIE77.0-E77.1
- •Refsum's diseaseG60.1
- •adrenoleukodystrophy [Addison-Schilder]E71.528
Related Codes(8)
Also Known As / Clinical Terms(142)
SNOMED CT
- Adult metachromatic leucodystrophy24326000
- Adult metachromatic leukodystrophy24326000
- Metachromatic leucodystrophy, adult type24326000
- Metachromatic leukodystrophy, adult type24326000
- Metachromatic leucodystrophy, congenital type40802007
- Metachromatic leukodystrophy, congenital type40802007
- Juvenile metachromatic leucodystrophy44359008
- Metachromatic leucodystrophy, juvenile type44359008
- Metachromatic leukodystrophy, juvenile type44359008
- Scholz cerebral sclerosis44359008
- Scholz-Bielschowsky-Henneberg diffuse cerebral sclerosis44359008
- Greenfield disease47683004
- Late infantile metachromatic leucodystrophy47683004
- Metachromatic leucodystrophy, late infantile type47683004
- Metachromatic leukodystrophy, late infantile type47683004
- SAPI - Sphingolipid activator protein I deficiency68390005
- Saposin B deficiency68390005
- Sphingolipid activator protein 1 deficiency68390005
- Metachromatic leucodystrophy without arylsulphatase deficiency83832001
- Metachromatic leukodystrophy without arylsulfatase deficiency83832001
- ARSA - Arylsulfatase A deficiency238031009
- ARSA - Arylsulphatase A deficiency238031009
- Arylsulfatase A deficiency238031009
- Arylsulphatase A deficiency238031009
- Cerebroside sulfatase deficiency238031009
- Cerebroside sulphatase deficiency238031009
- Severe deficiency of arylsulfatase238031009
- Severe deficiency of arylsulphatase238031009
- Metachromatic leucodystrophy due to deficiency of cerebroside sulphatase activator297278001
- Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator297278001
- Familial progressive cerebral sclerosis396338004
- MLD - Metachromatic leucodystrophy396338004
- Metachromatic leucodystrophy396338004
- Metachromatic leukodystrophy396338004
- Metachromatic leukoencephaly396338004
- Sulfatide lipidosis396338004
- Sulphatide lipidosis396338004
- van Bogaert-Nijssen disease396338004
- PMLD - Pelizaeus Merzbacher like disease717042001
- Pelizaeus Merzbacher like disease717042001
- Dystonia due to metachromatic leucodystrophy1260391004
- Dystonia due to metachromatic leukodystrophy1260391004
UMLS
- ARYLSULFATASE A DEFIC DISC0023522
- Arylsulfatase A Deficiency DiseaseC0023522
- CEREBRAL SCLEROSIS, DIFFUSE, METACHROMATIC FORMC0023522
- CEREBROSIDE SULFATASE DEFICIENCYC0023522
- CEREBROSIDE SULPHATASE DEFIC DISC0023522
- Cerebral sclerosis, Diffuse, Metachromatic FormC0023522
- Cerebral sclerosis, diffuse, metachromatic formC0023522
- Cerebroside Sulphatase Deficiency DiseaseC0023522
- Cerebroside sulphatase deficiency diseaseC0023522
- Familial progressive cerebral sclerosisC0023522
- Leukodystrophies, MetachromaticC0023522
- Leukodystrophy, MetachromaticC0023522
- Leukoencephalopathies, MetachromaticC0023522
- Leukoencephalopathy, MetachromaticC0023522
- Lipidosis, SulfatideC0023522
- METACHROMATIC LEUKODYSTROPHYC0023522
- METACHROMATIC LEUKOENCEPHALOPATHYC0023522
- MLDC0023522
- MLD - Metachromatic leucodystrophyC0023522
- Metachromatic LeukodystrophiesC0023522
- Metachromatic LeukodystrophyC0023522
- Metachromatic LeukoencephalopathiesC0023522
- Metachromatic LeukoencephalopathyC0023522
- Metachromatic leucodystrophyC0023522
- Metachromatic leucodystrophy (disorder)C0023522
- Metachromatic leukodystrophyC0023522
- Metachromatic leukoencephalopathyC0023522
- Metachromatic leukoencephalyC0023522
- SULFATIDE LIPIDOSISC0023522
- Scholz cerebral sclerosisC0023522
- Scholz-Bielschowsky-Henneberg diffuse cerebral sclerosisC0023522
- Sulfatide LipidosisC0023522
- Sulfatide lipidosisC0023522
- Sulphatide lipidosisC0023522
- leukodystrophy metachromaticC0023522
- metachromatic leucodystrophyC0023522
- metachromatic leukodystrophyC0023522
- metachromatic leukoencephalopathyC0023522
- metachromatic leukoencephalyC0023522
- mldC0023522
- sulfatide lipoidosisC0023522
- van Bogaert-Nijssen diseaseC0023522
Clinical Terms
- Sphingolipid activator protein 1 deficiency
- Adult metachromatic leukodystrophy
- Metachromatic leucodystrophy due to deficiency of cerebroside sulphatase activator
- ARYLSULFATASE A DEFIC DIS
- mld
- MLD - Metachromatic leucodystrophy
- CEREBROSIDE SULPHATASE DEFIC DIS
- Late infantile metachromatic leucodystrophy
- metachromatic leukoencephalopathy
- metachromatic leucodystrophy
- Metachromatic leucodystrophy, adult type
- Metachromatic leukodystrophy, congenital type
- leukodystrophy metachromatic
- Metachromatic leukodystrophy, adult type
- Leukoencephalopathy, Metachromatic
- Greenfield disease
- Arylsulfatase A deficiency
- Cerebral sclerosis, Diffuse, Metachromatic Form
- SAPI - Sphingolipid activator protein I deficiency
- Scholz cerebral sclerosis
- Familial progressive cerebral sclerosis
- PMLD - Pelizaeus Merzbacher like disease
- Arylsulphatase A deficiency
- Metachromatic leucodystrophy, congenital type
- Sulphatide lipidosis
- CEREBROSIDE SULFATASE DEFICIENCY
- van Bogaert-Nijssen disease
- Cerebroside sulphatase deficiency disease
- Arylsulfatase A Deficiency Disease
- Adult metachromatic leucodystrophy
- ARSA - Arylsulphatase A deficiency
- ARSA - Arylsulfatase A deficiency
- Dystonia due to metachromatic leukodystrophy
- Metachromatic leucodystrophy (disorder)
- Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
- Leukoencephalopathies, Metachromatic
- Dystonia due to metachromatic leucodystrophy
- Juvenile metachromatic leucodystrophy
- Metachromatic Leukodystrophies
- Sulfatide Lipidosis
- Metachromatic leucodystrophy, juvenile type
- Pelizaeus Merzbacher like disease
- Metachromatic Leukoencephalopathies
- Metachromatic leukodystrophy, late infantile type
- Cerebroside sulphatase deficiency
- Metachromatic leucodystrophy without arylsulphatase deficiency
- Metachromatic leukoencephaly
- Metachromatic leucodystrophy, late infantile type
- Scholz-Bielschowsky-Henneberg diffuse cerebral sclerosis
- Leukodystrophies, Metachromatic
- Metachromatic leukodystrophy, juvenile type
- Severe deficiency of arylsulphatase
- Leukodystrophy, Metachromatic
- Severe deficiency of arylsulfatase
- Metachromatic leukodystrophy without arylsulfatase deficiency
- Lipidosis, Sulfatide
- sulfatide lipoidosis
- Saposin B deficiency
Frequently Asked Questions
What is the ICD-10 code for metachromatic leukodystrophy?
The ICD-10-CM code for metachromatic leukodystrophy is E75.25. The full clinical description is "Metachromatic leukodystrophy". E75.25 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E75.25 mean?
ICD-10-CM code E75.25 represents “Metachromatic leukodystrophy”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E75.25 a billable code?
Yes, E75.25 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E75.25 in?
E75.25 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E75.25?
E75.25 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 6 more.
What SNOMED CT codes does E75.25 map to?
E75.25 maps to 11 SNOMED CT concepts: 238031009, 24326000, 1260391004, 396338004, 47683004, and 6 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E75.25?
E75.25 is linked to 1 UMLS Concept Unique Identifier: C0023522. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E75.25 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like metachromatic leukodystrophy 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 E75.25?
There is no direct ICD-11 mapping available for E75.25 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.
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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.