E75.01
BillableSandhoff disease
Sandhoff 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)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- GM>2< gangliosidosis, type 39537004
- Juvenile GM2 gangliosidosis9537004
- GM>2< gangliosidosis, type 223849003
- Hexosaminidase A AND B deficiency23849003
- O variant23849003
- Sandhoff disease23849003
- Total hexosaminidase deficiency23849003
- Adult chronic GM2 gangliosidosis49562005
- Infantile GM2 gangliosidosis62440002
- Total hexosaminidase deficiency - infantile238018004
- Total hexosaminidase deficiency - juvenile238019007
- Total hexosaminidase deficiency - adult238020001
UMLS
- DEFIC DIS HEXOSAMINIDASE A AND BC0036161
- Deficiency Disease, Hexosaminidase A and BC0036161
- Disease, Sandhoff-Jatzkewitz-PilzC0036161
- G(M2) Gangliosidosis, Type IIC0036161
- GANGLIOSIDOSIS GM2 TYPE IIC0036161
- GM2 GANGLIOSIDOSIS TYPE IIC0036161
- GM2 Gangliosidosis, Type 2C0036161
- GM2 Gangliosidosis, Type IIC0036161
- GM2 gangliosidosis, type 2C0036161
- GM2 gangliosidosis, type IIC0036161
- GM2-GANGLIOSIDOSIS, TYPE IIC0036161
- GM2-Gangliosidoses, Type IIC0036161
- GM2-Gangliosidosis, Type IIC0036161
- GM<sub>2</sub> gangliosidosis, type 2C0036161
- GM>2< gangliosidosis, type 2C0036161
- Gangliosidosis G(M2), Type IIC0036161
- Gangliosidosis GM2, Type IIC0036161
- HEXOSAMINIDASE A AND B DEFIC DISC0036161
- HEXOSAMINIDASES A AND B DEFICIENCYC0036161
- Hexosaminidase A AND B deficiencyC0036161
- Hexosaminidase A and B Deficiency DiseaseC0036161
- Hexosaminidase A and B deficiency diseaseC0036161
- Hexosaminidases A And B DeficiencyC0036161
- O variantC0036161
- SANDHOFF DISC0036161
- SANDHOFF DISEASEC0036161
- SANDHOFFS DISC0036161
- Sandhoff DiseaseC0036161
- Sandhoff Jatzkewitz Pilz DiseaseC0036161
- Sandhoff Jatzkewitz diseaseC0036161
- Sandhoff diseaseC0036161
- Sandhoff disease (disorder)C0036161
- Sandhoff's DiseaseC0036161
- Sandhoff-Jatzkewitz-Pilz DiseaseC0036161
- Sandhoff-Jatzkewitz-Pilz diseaseC0036161
- Sandhoffs DiseaseC0036161
- Total hexosaminidase deficiencyC0036161
- Type II GM2-GangliosidosesC0036161
- Type II GM2-GangliosidosisC0036161
- gangliosidosis GM2 type IIC0036161
- hexosaminidase a and b deficiencyC0036161
- sandhoff diseaseC0036161
- sandhoff's diseaseC0036161
- sandhoffs diseaseC0036161
Frequently Asked Questions
What is the ICD-10 code for sandhoff disease?
The ICD-10-CM code for sandhoff disease is E75.01. The full clinical description is "Sandhoff disease". E75.01 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E75.01 mean?
ICD-10-CM code E75.01 represents "Sandhoff 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 E75.01 a billable code?
Yes, E75.01 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E75.01 in?
E75.01 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E75.01?
E75.01 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 5 more.
What SNOMED CT codes does E75.01 map to?
E75.01 maps to 7 SNOMED CT concepts: 49562005, 23849003, 9537004, 62440002, 238020001, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E75.01?
E75.01 is linked to 1 UMLS Concept Unique Identifier: C0036161. 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.