E75.19
BillableOther gangliosidosis
Other gangliosidosis
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- GM1 gangliosidosis
- GM3 gangliosidosis
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
- GM1 Gangliosidosis type II18756002
- GM1 gangliosidosis, type 218756002
- Juvenile GM1 gangliosidosis18756002
- GM1 gangliosidosis238025006
- Deficiency of beta-galactosidase isoenzymes A, B AND C238026007
- GM>1< gangliosidosis, type 1238026007
- Generalised gangliosidosis238026007
- Generalized gangliosidosis238026007
- Infantile GM1 gangliosidosis238026007
- Infantile GM>1< gangliosidosis238026007
- Infantile gangliosidosis with bony involvement238026007
- Adult GM1 gangliosidosis238027003
- GM1 Gangliosidosis type III238027003
UMLS
- BETA GALACTOSIDASE 1 DEFICC0085131
- BETA-GALACTOSIDASE-1 DEFICIENCYC0085131
- Beta Galactosidase 1 Deficiency DiseaseC0085131
- Beta GalactosidosisC0085131
- Beta-Galactosidase-1 Deficiency DiseaseC0085131
- Beta-GalactosidosisC0085131
- Beta-galactosidase-1 deficiencyC0085131
- G(M1) GangliosidosisC0085131
- GLB1 DEFICIENCYC0085131
- GM1 GangliosidosisC0085131
- GM1 gangliosidosisC0085131
- GM1 gangliosidosis (disorder)C0085131
- Gangliosidosis G(M1)C0085131
- Gangliosidosis GM1C0085131
- Gangliosidosis, GM1C0085131
- Landing syndromeC0085131
- caffey syndromeC0085131
- gangliosidosis GM1C0085131
- gangliosidosis gm1C0085131
- gm1 gangliosidosisC0085131
- GM3 gangliosidosisC0795951
- Other GangliosidosisC0348488
- Other gangliosidosisC0348488
Frequently Asked Questions
What is the ICD-10 code for other gangliosidosis?
The ICD-10-CM code for other gangliosidosis is E75.19. The full clinical description is "Other gangliosidosis". E75.19 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E75.19 mean?
ICD-10-CM code E75.19 represents "Other gangliosidosis". 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 E75.19 a billable code?
Yes, E75.19 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E75.19 in?
E75.19 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E75.19?
E75.19 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 E75.19 map to?
E75.19 maps to 4 SNOMED CT concepts: 238027003, 238026007, 18756002, 238025006. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E75.19?
E75.19 is linked to 3 UMLS Concept Unique Identifiers: C0085131, C0795951, C0348488. 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.