E75.23
BillableKrabbe disease
Krabbe disease
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- mucolipidosis, types I-III (E77.0-E77.1)
- Refsum's disease (G60.1)
- adrenoleukodystrophy [Addison-Schilder] (E71.528)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Adult type Krabbe disease41142009
- Adult-type Krabbe's disease41142009
- Adult-type globoid cell leukodystrophy41142009
- Galactocerebroside beta-galactosidase deficiency - late onset41142009
- Globoid cell leucodystrophy late onset41142009
- Globoid cell leucodystrophy, late-onset41142009
- Globoid cell leukodystrophy, late-onset41142009
- Late onset Krabbe disease41142009
- Diffuse globoid cell cerebral sclerosis192782005
- GCL - Globoid cell leucodystrophy192782005
- Galactocerebroside beta-galactosidase deficiency192782005
- Galactosylceramide beta-galactosidase deficiency192782005
- Globoid cell leucodystrophy192782005
- Krabbe disease192782005
- Krabbe leucodystrophy192782005
- Krabbe's disease192782005
- Krabbe's leukodystrophy192782005
- Galactocerebroside beta-galactosidase deficiency - early onset238030005
- Infantile Krabbe disease238030005
- Atypical Krabbe disease due to saposin A deficiency1296731001
UMLS
- Cell Leukodystrophies, GloboidC0023521
- Cell Leukodystrophy, GloboidC0023521
- Cell Leukoencephalopathies, GloboidC0023521
- Cell Leukoencephalopathy, GloboidC0023521
- Deficiencies, GALCC0023521
- Deficiencies, GalactocerebrosidaseC0023521
- Deficiencies, Galactosylceramide beta-GalactosidaseC0023521
- Deficiency Disease, GalactosylceramidaseC0023521
- Deficiency Disease, Galactosylceramide-beta-GalactosidaseC0023521
- Deficiency Diseases, GalactosylceramidaseC0023521
- Deficiency Diseases, Galactosylceramide-beta-GalactosidaseC0023521
- Deficiency, GALCC0023521
- Deficiency, GalactocerebrosidaseC0023521
- Deficiency, Galactosylceramide beta-GalactosidaseC0023521
- Diffuse Globoid Body SclerosisC0023521
- Diffuse globoid body sclerosisC0023521
- Diffuse globoid cell cerebral sclerosisC0023521
- Disease, Galactosylceramidase DeficiencyC0023521
- Disease, Galactosylceramide-beta-Galactosidase DeficiencyC0023521
- Diseases, Galactosylceramidase DeficiencyC0023521
- Diseases, Galactosylceramide-beta-Galactosidase DeficiencyC0023521
- GALACTOCEREBROSIDASE DEFICIENCYC0023521
- GALACTOSYLCERAMIDASE DEFIC DISC0023521
- GALACTOSYLCERAMIDE BETA-GALACTOSIDASE DEFICIENCYC0023521
- GALC DEFICIENCYC0023521
- GALC DeficienciesC0023521
- GALC DeficiencyC0023521
- GALC deficiencyC0023521
- GCLC0023521
- GCL - Globoid cell leucodystrophyC0023521
- GLDC0023521
- GLOBOID CELL LEUKODYSTROPHYC0023521
- GLOBOID CELL LEUKOENCEPHALOPATHYC0023521
- Galactocerebrosidase DeficienciesC0023521
- Galactocerebrosidase DeficiencyC0023521
- Galactocerebroside beta-galactosidase deficiencyC0023521
- Galactosylceramidase Deficiency DiseaseC0023521
- Galactosylceramidase Deficiency DiseasesC0023521
- Galactosylceramidase deficiency diseaseC0023521
- Galactosylceramide LipidosisC0023521
- Galactosylceramide beta Galactosidase DeficiencyC0023521
- Galactosylceramide beta Galactosidase Deficiency DiseaseC0023521
- Galactosylceramide beta-Galactosidase DeficienciesC0023521
- Galactosylceramide beta-Galactosidase DeficiencyC0023521
- Galactosylceramide beta-galactosidase deficiencyC0023521
- Galactosylceramide beta-galactosidase deficiency (disorder)C0023521
- Galactosylceramide lipidosisC0023521
- Galactosylceramide-beta-Galactosidase Deficiency DiseaseC0023521
- Galactosylceramide-beta-Galactosidase Deficiency DiseasesC0023521
- Galactosylcerebrosidase DeficiencyC0023521
- Galactosylcerebrosidase deficiencyC0023521
- Galactosylsphingosine LipidosisC0023521
- Galactosylsphingosine lipidosisC0023521
- Globoid Body Sclerosis, DiffuseC0023521
- Globoid Cell LeukodystrophiesC0023521
- Globoid Cell LeukodystrophyC0023521
- Globoid Cell LeukoencephalopathiesC0023521
- Globoid Cell LeukoencephalopathyC0023521
- Globoid LeukodystrophiesC0023521
- Globoid LeukodystrophyC0023521
- Globoid cell leucodystrophyC0023521
- KRABBE DISC0023521
- KRABBE DISEASEC0023521
- KRABBES DISC0023521
- KRBC0023521
- Krabbe DiseaseC0023521
- Krabbe LeukodystrophyC0023521
- Krabbe diseaseC0023521
- Krabbe leucodystrophyC0023521
- Krabbe's DiseaseC0023521
- Krabbe's LeukodystrophyC0023521
- Krabbe's diseaseC0023521
- Krabbe's leukodystrophyC0023521
- Krabbes DiseaseC0023521
- Krabbes LeukodystrophyC0023521
- Leukodystrophies, GloboidC0023521
- Leukodystrophies, Globoid CellC0023521
- Leukodystrophy, GloboidC0023521
- Leukodystrophy, Globoid CellC0023521
- Leukodystrophy, KrabbeC0023521
- Leukodystrophy, Krabbe'sC0023521
- Leukoencephalopathies, Globoid CellC0023521
- Leukoencephalopathy, Globoid CellC0023521
- Psychosine LipidosisC0023521
- Psychosine lipidosisC0023521
- beta galactocerebrosidase deficiencyC0023521
- beta-Galactosidase Deficiencies, GalactosylceramideC0023521
- beta-Galactosidase Deficiency, GalactosylceramideC0023521
- disease krabbeC0023521
- disease krabbesC0023521
- diseases krabbeC0023521
- galactosylceramide lipidosisC0023521
- globoid cell leukodystrophyC0023521
- globoid leukodystrophyC0023521
- krabbe diseaseC0023521
- krabbe leukodystrophyC0023521
- krabbe's diseaseC0023521
- krabbe's leukodystrophyC0023521
- krabbes diseaseC0023521
- leukodystrophy krabbeC0023521
Frequently Asked Questions
What is the ICD-10 code for krabbe disease?
The ICD-10-CM code for krabbe disease is E75.23. The full clinical description is "Krabbe disease". E75.23 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E75.23 mean?
ICD-10-CM code E75.23 represents "Krabbe disease". 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 E75.23 a billable code?
Yes, E75.23 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E75.23 in?
E75.23 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E75.23?
E75.23 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 E75.23 map to?
E75.23 maps to 4 SNOMED CT concepts: 41142009, 1296731001, 192782005, 238030005. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E75.23?
E75.23 is linked to 1 UMLS Concept Unique Identifier: C0023521. 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.