E75.240
BillableNiemann-Pick disease type A
Niemann-Pick disease type A
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Acid sphingomyelinase deficiency type A (ASMD type A)
- Infantile neurovisceral acid sphingomyelinase deficiency
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)
- adrenoleukodystrophy [Addison-Schilder] (E71.528)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Lipoidosis11455007
- Classical Niemann-Pick disease52165006
- Niemann-Pick disease neuropathic type52165006
- Niemann-Pick disease type A52165006
- Niemann-Pick disease, acute neuropathic form52165006
- Niemann-Pick disease, acute neurovisceral form52165006
- Niemann-Pick disease, type A52165006
- Neuronal cholesterol lipidosis58459009
- Niemann-Pick disease58459009
- Sphingomyelin lipidosis58459009
- Sphingomyelin/cholesterol lipidosis58459009
- Sphingomyelinase deficiency58459009
UMLS
- ACID SPHINGOMYELINASE DEFICIENCY, NEUROVISCERAL TYPEC0268242
- ASMD, NEUROVISCERAL TYPEC0268242
- CLASSICAL NIEMANN PICK DISC0268242
- Cholesterol Lipidoses, NeuronalC0268242
- Cholesterol Lipidoses, SphingomyelinC0268242
- Cholesterol Lipidosis, NeuronalC0268242
- Cholesterol Lipidosis, SphingomyelinC0268242
- Classical Niemann Pick DiseaseC0268242
- Classical Niemann-Pick DiseaseC0268242
- Classical Niemann-Pick diseaseC0268242
- Deficiencies, SphingomyelinaseC0268242
- Deficiency, SphingomyelinaseC0268242
- Infantile neurovisceral acid sphingomyelinase deficiencyC0268242
- Lipidoses, Neuronal CholesterolC0268242
- Lipidoses, SphingomyelinC0268242
- Lipidoses, Sphingomyelin CholesterolC0268242
- Lipidosis, Neuronal CholesterolC0268242
- Lipidosis, SphingomyelinC0268242
- Lipidosis, Sphingomyelin CholesterolC0268242
- NIEMANN PICK DIS ACUTE NEURONOPATHIC FORMC0268242
- NIEMANN PICK DIS ACUTE NEUROVISCERAL FORMC0268242
- NIEMANN PICK DIS NEURONOPATHIC TYPEC0268242
- NIEMANN PICK DIS TYPE AC0268242
- NIEMANN PICKS DIS TYPE AC0268242
- NIEMANN-PICK DISEASE, TYPE AC0268242
- Neuronal Cholesterol LipidosesC0268242
- Neuronal Cholesterol LipidosisC0268242
- Niemann Pick Disease, Acute Neuronopathic FormC0268242
- Niemann Pick Disease, Acute Neurovisceral FormC0268242
- Niemann Pick Disease, Neuronopathic TypeC0268242
- Niemann Pick Disease, Type AC0268242
- Niemann Pick's Disease Type AC0268242
- Niemann-Pick Disease, Acute Neuronopathic FormC0268242
- Niemann-Pick Disease, Acute Neurovisceral FormC0268242
- Niemann-Pick Disease, ClassicalC0268242
- Niemann-Pick Disease, Neuronopathic TypeC0268242
- Niemann-Pick Disease, Type AC0268242
- Niemann-Pick disease neuropathic typeC0268242
- Niemann-Pick disease type AC0268242
- Niemann-Pick disease, acute neuropathic formC0268242
- Niemann-Pick disease, acute neurovisceral formC0268242
- Niemann-Pick disease, type AC0268242
- Niemann-Pick disease, type A (disorder)C0268242
- Niemann-Pick's Disease Type AC0268242
- Ophthalmoplegia, Supraoptic VerticalC0268242
- Ophthalmoplegias, Supraoptic VerticalC0268242
- SPHINGOMYELIN LIPIDOSISC0268242
- SPHINGOMYELINASE DEFIC DISC0268242
- SPHINGOMYELINASE DEFICIENCYC0268242
- Sphingomyelin Cholesterol LipidosesC0268242
- Sphingomyelin Cholesterol LipidosisC0268242
- Sphingomyelin LipidosesC0268242
- Sphingomyelin LipidosisC0268242
- Sphingomyelinase DeficienciesC0268242
- Sphingomyelinase DeficiencyC0268242
- Sphingomyelinase Deficiency DiseaseC0268242
- Sphingomyelinase Deficiency DiseasesC0268242
- Supraoptic Vertical OphthalmoplegiaC0268242
- Supraoptic Vertical OphthalmoplegiasC0268242
- TYPE A NIEMANN PICK DISC0268242
- Type A Niemann Pick DiseaseC0268242
- Type A Niemann-Pick DiseaseC0268242
- Vertical Ophthalmoplegia, SupraopticC0268242
- Vertical Ophthalmoplegias, SupraopticC0268242
- niemann-pick disease typeC0268242
- niemann-pick disease type aC0268242
- Acid sphingomyelinase deficiency type A (ASMD type A)C5539328
Frequently Asked Questions
What is the ICD-10 code for niemann-pick disease type a?
The ICD-10-CM code for niemann-pick disease type a is E75.240. The full clinical description is "Niemann-Pick disease type A". E75.240 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E75.240 mean?
ICD-10-CM code E75.240 represents "Niemann-Pick disease type A". 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 E75.240 a billable code?
Yes, E75.240 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E75.240 in?
E75.240 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E75.240?
E75.240 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 6 more.
What SNOMED CT codes does E75.240 map to?
E75.240 maps to 3 SNOMED CT concepts: 52165006, 11455007, 58459009. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E75.240?
E75.240 is linked to 2 UMLS Concept Unique Identifiers: C0268242, C5539328. 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.