E75.02
BillableTay-Sachs disease
Tay-Sachs 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(130)
SNOMED CT
- AB variant71253000
- GM2 activator deficiency71253000
- GM>2< gangliosidosis, type AB71253000
- Hexosaminidase activator deficiency71253000
- Tay-Sachs disease, variant AB71253000
- Amaurotic familial idiocy111385000
- GM2 gangliosidosis, B, B1 variant111385000
- Hexosaminidase A deficiency111385000
- Infantile amaurotic familial disease111385000
- Severe hexosaminidase A deficiency111385000
- Tay-Sachs disease111385000
- B variant hexosaminidase A deficiency192787004
- B variant hexosaminidase A deficiency - infantile238021002
- B variant hexosaminidase A deficiency - juvenile238022009
- B variant hexosaminidase A deficiency - adult238023004
- B1 variant hexosaminidase A deficiency238024005
UMLS
- B VARIANT GM2-GANGLIOSIDOSISC0039373
- B Variant GM2 GangliosidosisC0039373
- B Variant GM2-GangliosidosesC0039373
- B Variant GM2-GangliosidosisC0039373
- B variant GM2 gangliosidosisC0039373
- DEFIC DIS HEXOSAMINIDASE AC0039373
- Deficiency Disease Hexosaminidase AC0039373
- G(M2) Gangliosidosis, Type IC0039373
- GANGLIOSIDOSIS GM2 TYPE IC0039373
- GM2 GANGLIOSIDOSIS TYPE IC0039373
- GM2 Gangliosidosis, B VariantC0039373
- GM2 Gangliosidosis, Type 1C0039373
- GM2 Gangliosidosis, Type IC0039373
- GM2 gangliosidosis, B, B1 variantC0039373
- GM2 gangliosidosis, type 1C0039373
- GM2-GANGLIOSIDOSIS, TYPE IC0039373
- GM2-Gangliosidosis, B VariantC0039373
- GM2-Gangliosidosis, Type IC0039373
- Gangliosidosis G(M2), Type IC0039373
- Gangliosidosis GM2 , Type 1C0039373
- Gangliosidosis GM2, B VariantC0039373
- Gangliosidosis GM2, Type IC0039373
- HEXA DEFICIENCYC0039373
- HEXOSAMINIDASE A DEFIC DISC0039373
- HEXOSAMINIDASE A DEFICIENCYC0039373
- Hexosaminidase A Deficiency DiseaseC0039373
- Hexosaminidase A deficiencyC0039373
- Severe hexosaminidase A deficiencyC0039373
- Sphingolipidosis, Tay SachsC0039373
- Sphingolipidosis, Tay-SachsC0039373
- TAY SACHS DISC0039373
- TAY-SACHS DISEASEC0039373
- TSDC0039373
- Tay Sachs DiseaseC0039373
- Tay Sachs Disease, B VariantC0039373
- Tay Sachs diseaseC0039373
- Tay-Sachs DiseaseC0039373
- Tay-Sachs Disease, B VariantC0039373
- Tay-Sachs SphingolipidosisC0039373
- Tay-Sachs diseaseC0039373
- Tay-Sachs disease (disorder)C0039373
- Type I GM2-GangliosidosisC0039373
- deficiency hexosaminidaseC0039373
- disease sach tayC0039373
- disease sach's tayC0039373
- disease sachs tayC0039373
- disease tay sachC0039373
- disease tay sachsC0039373
- disease tay-sachsC0039373
- diseases sachs tayC0039373
- diseases sachs taysC0039373
- diseases tay sachsC0039373
- gangliosidosis GM2 type IC0039373
- hexosaminidase A deficiencyC0039373
- tay sach's diseaseC0039373
- tay sachs diseaseC0039373
- tay-sachs diseaseC0039373
- tsdC0039373
Clinical Terms
- GM2-GANGLIOSIDOSIS, TYPE I
- disease tay sach
- disease tay-sachs
- B VARIANT GM2-GANGLIOSIDOSIS
- GM2 Gangliosidosis, B Variant
- Sphingolipidosis, Tay Sachs
- B variant hexosaminidase A deficiency - juvenile
- GM>2< gangliosidosis, type AB
- TAY SACHS DIS
- Tay-Sachs disease, variant AB
- disease sachs tay
- Hexosaminidase A deficiency
- B variant hexosaminidase A deficiency
- Tay-Sachs Sphingolipidosis
- DEFIC DIS HEXOSAMINIDASE A
- tay sach's disease
- AB variant
- Infantile amaurotic familial disease
- Gangliosidosis GM2, Type I
- GM2 gangliosidosis, B, B1 variant
- Hexosaminidase A Deficiency Disease
- disease sach's tay
- Amaurotic familial idiocy
- GANGLIOSIDOSIS GM2 TYPE I
- deficiency hexosaminidase
- disease tay sachs
- G(M2) Gangliosidosis, Type I
- GM2 Gangliosidosis, Type 1
- B1 variant hexosaminidase A deficiency
- Tay Sachs Disease
- B variant hexosaminidase A deficiency - adult
- Tay-Sachs Disease, B Variant
- GM2-Gangliosidosis, B Variant
- Hexosaminidase activator deficiency
- B variant GM2 gangliosidosis
- GM2 GANGLIOSIDOSIS TYPE I
- Type I GM2-Gangliosidosis
- disease sach tay
- Tay Sachs Disease, B Variant
- Severe hexosaminidase A deficiency
- Gangliosidosis G(M2), Type I
- Sphingolipidosis, Tay-Sachs
- Deficiency Disease Hexosaminidase A
- B Variant GM2-Gangliosidoses
- Gangliosidosis GM2, B Variant
- HEXA DEFICIENCY
- Tay-Sachs disease (disorder)
- tsd
- GM2 activator deficiency
- GM2 Gangliosidosis, Type I
- Gangliosidosis GM2 , Type 1
- B variant hexosaminidase A deficiency - infantile
- HEXOSAMINIDASE A DEFIC DIS
- diseases sachs tay
- diseases sachs tays
- diseases tay sachs
Frequently Asked Questions
What is the ICD-10 code for tay-sachs disease?
The ICD-10-CM code for tay-sachs disease is E75.02. The full clinical description is "Tay-Sachs disease". E75.02 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E75.02 mean?
ICD-10-CM code E75.02 represents “Tay-Sachs 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 E75.02 a billable code?
Yes, E75.02 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E75.02 in?
E75.02 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E75.02?
E75.02 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 E75.02 map to?
E75.02 maps to 7 SNOMED CT concepts: 71253000, 111385000, 192787004, 238023004, 238021002, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E75.02?
E75.02 is linked to 1 UMLS Concept Unique Identifier: C0039373. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E75.02 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like tay-sachs 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 E75.02?
There is no direct ICD-11 mapping available for E75.02 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.