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 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
Related Codes(3)
Also Known As / Clinical Terms(93)
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
Clinical Terms
- Deficiency Disease, Hexosaminidase A and B
- Sandhoff Jatzkewitz disease
- GM2-Gangliosidosis, Type II
- gangliosidosis GM2 type II
- GM2 GANGLIOSIDOSIS TYPE II
- Sandhoffs Disease
- Type II GM2-Gangliosidosis
- Juvenile GM2 gangliosidosis
- HEXOSAMINIDASES A AND B DEFICIENCY
- Sandhoff Jatzkewitz Pilz Disease
- GM2 gangliosidosis, type II
- GM2 Gangliosidosis, Type 2
- Type II GM2-Gangliosidoses
- SANDHOFFS DIS
- DEFIC DIS HEXOSAMINIDASE A AND B
- Gangliosidosis GM2, Type II
- O variant
- Sandhoff-Jatzkewitz-Pilz disease
- Sandhoff disease (disorder)
- Disease, Sandhoff-Jatzkewitz-Pilz
- HEXOSAMINIDASE A AND B DEFIC DIS
- Hexosaminidase A AND B deficiency
- Total hexosaminidase deficiency - juvenile
- GM2-Gangliosidoses, Type II
- G(M2) Gangliosidosis, Type II
- Total hexosaminidase deficiency
- GM>2< gangliosidosis, type 2
- Total hexosaminidase deficiency - adult
- Infantile GM2 gangliosidosis
- Hexosaminidase A and B deficiency disease
- GM<sub>2</sub> gangliosidosis, type 2
- Sandhoff's Disease
- GM>2< gangliosidosis, type 3
- SANDHOFF DIS
- Total hexosaminidase deficiency - infantile
- Gangliosidosis G(M2), Type II
- Adult chronic GM2 gangliosidosis
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.
How does E75.01 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like sandhoff 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 E75.01?
There is no direct ICD-11 mapping available for E75.01 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.