AutoICD API

E75.22

Billable

Gaucher disease

Gaucher disease

Status

Billable / Specific

Block

E70-E88

Parent Code

E75.2

Coding Notes

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(8)
E75.21

Fabry (-Anderson) disease

BillableE75.23

Krabbe disease

BillableE75.24

Niemann-Pick disease

E75.25

Metachromatic leukodystrophy

BillableE75.26

Sulfatase deficiency

BillableE75.27

Pelizaeus-Merzbacher disease

BillableE75.28

Canavan disease

BillableE75.29

Other sphingolipidosis

Billable
Also Known As / Clinical Terms(254)

SNOMED CT

UMLS

Clinical Terms

  • Infantile Gaucher disease
  • Infantile Gaucher's disease
  • GAUCHER DIS
  • Lipoid Histiocytosis (Kerasin Type)
  • Disease, Glucocerebrosidase Deficiency
  • ACID BETA GLUCOSIDASE DEFIC DIS
  • familial splenic anemia
  • Glucosylceramide beta-glucosidase deficiency (disorder)
  • Disease, Gaucher's
  • Glucocerebrosidase Deficiency
  • Cerebroside Lipidoses, Glucosyl
  • Gaucher's disease, type III
  • Acid beta-Glucosidase Deficiency Disease
  • Glucocerebrosidase deficiency type I
  • Gauchers Disease
  • Cerebral degeneration in Gaucher's disease
  • Gaucher-like disease
  • Subacute neuronopathic Gaucher disease
  • Norrbottnian Gaucher disease
  • Kerasin Lipoidoses
  • Cerebroside Lipidosis, Glucosyl
  • Gaucher's disease, type I
  • Deficiency Disease, Glucocerebrosidase
  • Deficiencies, Glucocerebrosidase
  • Lipidosis Syndrome, Cerebroside
  • glucosylceramide lipidosis
  • Atypical Gaucher disease due to saposin C deficiency
  • Histiocytoses, Lipoid (Kerasin Type)
  • Lipoid Histiocytoses (Kerasin Type)
  • Noncerebral juvenile Gaucher's disease
  • Gaucher disease with ophthalmoplegia and cardiovascular calcification
  • Glucosylceramidase Deficiency
  • gaucher's disease
  • GLUCOCEREBROSIDASE DEFIC DIS
  • Glucosylceramide Beta-Glucosidase Deficiency
  • Cerebroside Lipidosis Syndrome
  • disease gaucher's
  • gaucher syndrome
  • Diseases, Gauchers
  • Cardiovascular Gaucher disease
  • Glucocerebrosidase deficiency type II
  • Perinatal lethal Gaucher disease
  • Chronic non-neuropathic Gaucher disease
  • Diseases, Glucocerebrosidase Deficiency
  • Syndromes, Cerebroside Lipidosis
  • Glucocerebrosidase Deficiency Disease
  • Subacute neuronopathic Gaucher's disease
  • Lipoidosis, Kerasin
  • Acute neuronopathic Gaucher disease
  • Lipoidoses, Kerasin
  • Cerebral acute Gaucher disease
  • Chronic non-neuropathic Gaucher's disease (disorder)
  • Kerasin thesaurismosis
  • Glucosylceramidase deficiency, acute type
  • Acid beta-Glucosidase Deficiency
  • Cerebroside Lipidosis Syndromes
  • Chronic adult Gaucher's disease
  • Cerebral degeneration in Gaucher disease
  • Lipidosis, Glucosyl Cerebroside
  • thesaurismoses, Kerasin
  • Glucocerebrosidosis
  • Glucocerebrosidase deficiency type III
  • Gauchers Diseases
  • Glucosyl Cerebroside Lipidosis
  • Infantile cerebral Gaucher's disease
  • Deficiency, Glucocerebrosidase
  • Glucocerebrosidoses
  • Glucosylceramidase deficiency, subacute type
  • Glucocerebrosidase Deficiency Diseases
  • Glucosyl Cerebroside Lipidoses
  • Gaucher disease type 2
  • Kerasin lipoidosis
  • Glucocerebrosidase Deficiencies
  • Disease, Gaucher
  • Histiocytoses, Kerasin
  • Kerasin thesaurismoses
  • Kerasin Histiocytosis
  • Glucosylceramide Lipidoses
  • Glucosylceramidase deficiency, chronic type
  • GLUCOSYLCERAMIDE BETA GLUCOSIDASE DEFIC DIS
  • Gaucher splenomegaly
  • Juvenile Gaucher disease
  • Gaucher's disease, type II
  • Deficiency Diseases, Glucocerebrosidase
  • Histiocytosis, Kerasin
  • GAUCHERS DIS
  • Adult Gaucher disease
  • Lipidoses, Glucosyl Cerebroside
  • Lipidosis, Glucosylceramide
  • Kerasin thesaurismosis (disorder)
  • Gaucher's disease type 3C
  • Acute cerebral Gaucher's disease
  • Juvenile Gaucher's disease
  • Glucosylceramide Beta-Glucosidase Deficiency Disease
  • Histiocytosis, Lipoid (Kerasin Type)
  • thesaurismosis, Kerasin
  • disease gauchers
  • Chronic non-neuropathic Gaucher's disease
  • Splenomegaly, Gaucher
  • Acute neuronopathic Gaucher's disease
  • Kerasin Histiocytoses
  • Syndrome, Gaucher
  • Disease, Gauchers
  • disease gaucher
  • Syndrome, Cerebroside Lipidosis
  • Lipidosis Syndromes, Cerebroside
  • Lipidoses, Glucosylceramide
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.

How does E75.22 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like gaucher disease 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 E75.22?

There is no direct ICD-11 mapping available for E75.22 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.