E75.22
BillableGaucher disease
Gaucher 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
- Gaucher's disease, type III5963005
- Glucocerebrosidase deficiency type III5963005
- Glucosylceramidase deficiency, subacute type5963005
- Juvenile Gaucher disease5963005
- Juvenile Gaucher's disease5963005
- Norrbottnian Gaucher disease5963005
- Subacute neuronopathic Gaucher disease5963005
- Subacute neuronopathic Gaucher's disease5963005
- Acute cerebral Gaucher's disease12246008
- Acute neuronopathic Gaucher disease12246008
- Acute neuronopathic Gaucher's disease12246008
- Cerebral acute Gaucher disease12246008
- Gaucher disease type 212246008
- Gaucher's disease, type II12246008
- Glucocerebrosidase deficiency type II12246008
- Glucosylceramidase deficiency, acute type12246008
- Infantile Gaucher disease12246008
- Infantile Gaucher's disease12246008
- Infantile cerebral Gaucher's disease12246008
- Adult Gaucher disease62201009
- Chronic adult Gaucher's disease62201009
- Chronic non-neuropathic Gaucher disease62201009
- Chronic non-neuropathic Gaucher's disease62201009
- Gaucher's disease, type I62201009
- Glucocerebrosidase deficiency type I62201009
- Glucosylceramidase deficiency, chronic type62201009
- Noncerebral juvenile Gaucher's disease62201009
- Kerasin thesaurismosis180485001
- Cerebroside lipidosis syndrome190794006
- Gaucher disease190794006
- Gaucher splenomegaly190794006
- Gaucher syndrome190794006
- Gaucher's disease190794006
- Glucocerebrosidase deficiency190794006
- Glucocerebrosidosis190794006
- Glucosylceramidase deficiency190794006
- Glucosylceramide beta-glucosidase deficiency190794006
- Kerasin histiocytosis190794006
- Kerasin lipoidosis190794006
- Cerebral degeneration in Gaucher disease192791009
- Cerebral degeneration in Gaucher's disease192791009
- Perinatal lethal Gaucher disease870313002
- Atypical Gaucher disease due to saposin C deficiency1156792000
- Cardiovascular Gaucher disease1156813002
- Gaucher disease with ophthalmoplegia and cardiovascular calcification1156813002
- Gaucher's disease type 3C1156813002
- Gaucher-like disease1156813002
UMLS
- ACID BETA GLUCOSIDASE DEFIC DISC0017205
- Acid beta-Glucosidase DeficiencyC0017205
- Acid beta-Glucosidase Deficiency DiseaseC0017205
- Adult Gaucher diseaseC0017205
- Cerebroside Lipidoses, GlucosylC0017205
- Cerebroside Lipidosis SyndromeC0017205
- Cerebroside Lipidosis SyndromesC0017205
- Cerebroside Lipidosis, GlucosylC0017205
- Cerebroside lipidosis syndromeC0017205
- Chronic adult Gaucher's diseaseC0017205
- Chronic non-neuropathic Gaucher diseaseC0017205
- Chronic non-neuropathic Gaucher's diseaseC0017205
- Chronic non-neuropathic Gaucher's disease (disorder)C0017205
- Deficiencies, GlucocerebrosidaseC0017205
- Deficiency Disease, GlucocerebrosidaseC0017205
- Deficiency Diseases, GlucocerebrosidaseC0017205
- Deficiency, GlucocerebrosidaseC0017205
- Disease, GaucherC0017205
- Disease, Gaucher'sC0017205
- Disease, GauchersC0017205
- Disease, Glucocerebrosidase DeficiencyC0017205
- Diseases, GauchersC0017205
- Diseases, Glucocerebrosidase DeficiencyC0017205
- GAUCHER DISC0017205
- GAUCHERS DISC0017205
- GLUCOCEREBROSIDASE DEFIC DISC0017205
- GLUCOSYLCERAMIDE BETA GLUCOSIDASE DEFIC DISC0017205
- Gaucher DiseaseC0017205
- Gaucher SplenomegalyC0017205
- Gaucher SyndromeC0017205
- Gaucher diseaseC0017205
- Gaucher splenomegalyC0017205
- Gaucher syndromeC0017205
- Gaucher's DiseaseC0017205
- Gaucher's diseaseC0017205
- Gauchers DiseaseC0017205
- Gauchers DiseasesC0017205
- Gauchers diseaseC0017205
- Glucocerebrosidase DeficienciesC0017205
- Glucocerebrosidase DeficiencyC0017205
- Glucocerebrosidase Deficiency DiseaseC0017205
- Glucocerebrosidase Deficiency DiseasesC0017205
- Glucocerebrosidase deficiencyC0017205
- GlucocerebrosidosesC0017205
- GlucocerebrosidosisC0017205
- Glucosyl Cerebroside LipidosesC0017205
- Glucosyl Cerebroside LipidosisC0017205
- Glucosyl cerebroside lipidosisC0017205
- Glucosylceramidase DeficiencyC0017205
- Glucosylceramidase deficiencyC0017205
- Glucosylceramidase deficiency, chronic typeC0017205
- Glucosylceramide Beta-Glucosidase DeficiencyC0017205
- Glucosylceramide Beta-Glucosidase Deficiency DiseaseC0017205
- Glucosylceramide LipidosesC0017205
- Glucosylceramide LipidosisC0017205
- Glucosylceramide beta-glucosidase deficiencyC0017205
- Glucosylceramide beta-glucosidase deficiency (disorder)C0017205
- Glucosylceramide lipidosisC0017205
- Histiocytoses, KerasinC0017205
- Histiocytoses, Lipoid (Kerasin Type)C0017205
- Histiocytosis, KerasinC0017205
- Histiocytosis, Lipoid (Kerasin Type)C0017205
- Kerasin HistiocytosesC0017205
- Kerasin HistiocytosisC0017205
- Kerasin LipoidosesC0017205
- Kerasin LipoidosisC0017205
- Kerasin histiocytosisC0017205
- Kerasin lipoidosisC0017205
- Kerasin thesaurismosesC0017205
- Kerasin thesaurismosisC0017205
- Kerasin thesaurismosis (disorder)C0017205
- Lipidoses, Glucosyl CerebrosideC0017205
- Lipidoses, GlucosylceramideC0017205
- Lipidosis Syndrome, CerebrosideC0017205
- Lipidosis Syndromes, CerebrosideC0017205
- Lipidosis, Glucosyl CerebrosideC0017205
- Lipidosis, GlucosylceramideC0017205
- Lipoid Histiocytoses (Kerasin Type)C0017205
- Lipoid Histiocytosis (Kerasin Type)C0017205
- Lipoid histiocytosis (kerasin type)C0017205
- Lipoidoses, KerasinC0017205
- Lipoidosis, KerasinC0017205
- Splenomegaly, GaucherC0017205
- Syndrome, Cerebroside LipidosisC0017205
- Syndrome, GaucherC0017205
- Syndromes, Cerebroside LipidosisC0017205
- disease gaucherC0017205
- disease gaucher'sC0017205
- disease gauchersC0017205
- familial splenic anemiaC0017205
- gaucher diseaseC0017205
- gaucher syndromeC0017205
- gaucher's diseaseC0017205
- gauchers diseaseC0017205
- glucocerebrosidosisC0017205
- glucosylceramidase deficiencyC0017205
- glucosylceramide lipidosisC0017205
- lipoid histiocytosis (kerasin type)C0017205
- thesaurismoses, KerasinC0017205
- thesaurismosis, KerasinC0017205
Frequently Asked Questions
What is the ICD-10 code for gaucher disease?
The ICD-10-CM code for gaucher disease is E75.22. The full clinical description is "Gaucher disease". E75.22 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E75.22 mean?
ICD-10-CM code E75.22 represents "Gaucher 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 E75.22 a billable code?
Yes, E75.22 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E75.22 in?
E75.22 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E75.22?
E75.22 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 E75.22 map to?
E75.22 maps to 9 SNOMED CT concepts: 12246008, 62201009, 1156792000, 1156813002, 192791009, and 4 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E75.22?
E75.22 is linked to 1 UMLS Concept Unique Identifier: C0017205. 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.