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 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
- 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
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.
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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.