{"code":"E75","type":"category","title":"Disorders of sphingolipid metabolism and other lipid storage disorders","codeAlso":[],"includes":[],"modern_v":"official26","codeFirst":[],"excludes1":["mucolipidosis, types I-III (E77.0-E77.1)","Refsum's disease (G60.1)","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)"],"excludes2":["Ehlers-Danlos syndromes (Q79.6-)"],"isBillable":false,"fyEffectivity":{"fy2026":true,"fy2027":true},"sibling_codes":["E75.0","E75.01","E75.02","E75.09","E75.1","E75.10","E75.11","E75.19","E75.2","E75.21","E75.22","E75.23","E75.24","E75.240","E75.241","E75.242","E75.243","E75.244","E75.248","E75.249","E75.25","E75.26","E75.27","E75.28","E75.29","E75.3","E75.4","E75.5","E75.6"],"inclusionTerms":[],"sibling_titles":{"code":"E75.6","title":"Lipid storage disorder, unspecified","isBillable":true},"useAdditionalCode":[],"clinicalDefinition":"Disorders of sphingolipid metabolism and other lipid storage disorders is a non-billable ICD-10-CM category code (E75). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","officialDefinition":"Disorders of sphingolipid metabolism and other lipid storage disorders is a non-billable ICD-10-CM category code (E75). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","seventhCharacterInstructions":[],"workflowProtocols":[],"guidelines":{"whenToUse":[],"whenNotToUse":[],"commonBillingMistakes":[],"codeComparisons":[],"documentationChecklist":[]},"domainLandscape":{"summary":"Primary diagnostic domain and clinical landscape evaluation.","keyCategories":[],"diagnosticContinuum":"Progression continuum from acute presentation to resolution."},"children":[{"code":"E75.0","title":"GM2 gangliosidosis","description":"GM2 gangliosidosis is a non-billable ICD-10-CM category code (E75.0). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":false,"slug":"e75.0-gm2-gangliosidosis"},{"code":"E75.00","title":"GM2 gangliosidosis, unspecified","description":"GM2 gangliosidosis, unspecified is a billable ICD-10-CM diagnosis code (E75.00). Excludes1 (not coded here): mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.00-gm2-gangliosidosis-unspecified"},{"code":"E75.01","title":"Sandhoff disease","description":"Sandhoff disease is a billable ICD-10-CM diagnosis code (E75.01). Excludes1 (not coded here): mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.01-sandhoff-disease"},{"code":"E75.02","title":"Tay-Sachs disease","description":"Tay-Sachs disease is a billable ICD-10-CM diagnosis code (E75.02). Excludes1 (not coded here): mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.02-tay-sachs-disease"},{"code":"E75.09","title":"Other GM2 gangliosidosis","description":"Other GM2 gangliosidosis is a billable ICD-10-CM diagnosis code (E75.09). Inclusion terms: Adult GM2 gangliosidosis; Juvenile GM2 gangliosidosis. Excludes1 (not coded here): mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.09-other-gm2-gangliosidosis"},{"code":"E75.1","title":"Other and unspecified gangliosidosis","description":"Other and unspecified gangliosidosis is a non-billable ICD-10-CM category code (E75.1). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":false,"slug":"e75.1-other-and-unspecified-gangliosidosis"},{"code":"E75.10","title":"Unspecified gangliosidosis","description":"Unspecified gangliosidosis is a billable ICD-10-CM diagnosis code (E75.10). Inclusion terms: Gangliosidosis NOS. Excludes1 (not coded here): mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.10-unspecified-gangliosidosis"},{"code":"E75.11","title":"Mucolipidosis IV","description":"Mucolipidosis IV is a billable ICD-10-CM diagnosis code (E75.11). Excludes1 (not coded here): mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.11-mucolipidosis-iv"},{"code":"E75.19","title":"Other gangliosidosis","description":"Other gangliosidosis is a billable ICD-10-CM diagnosis code (E75.19). Inclusion terms: GM1 gangliosidosis; GM3 gangliosidosis. Excludes1 (not coded here): mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.19-other-gangliosidosis"},{"code":"E75.2","title":"Other sphingolipidosis","description":"Other sphingolipidosis is a non-billable ICD-10-CM category code (E75.2). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":false,"slug":"e75.2-other-sphingolipidosis"},{"code":"E75.21","title":"Fabry (-Anderson) disease","description":"Fabry (-Anderson) disease is a billable ICD-10-CM diagnosis code (E75.21). Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.21-fabry-anderson-disease"},{"code":"E75.22","title":"Gaucher disease","description":"Gaucher disease is a billable ICD-10-CM diagnosis code (E75.22). Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.22-gaucher-disease"},{"code":"E75.23","title":"Krabbe disease","description":"Krabbe disease is a billable ICD-10-CM diagnosis code (E75.23). Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.23-krabbe-disease"},{"code":"E75.24","title":"Niemann-Pick disease","description":"Niemann-Pick disease is a non-billable ICD-10-CM category code (E75.24). A more specific billable subcode must be selected for claims submission. Inclusion terms: Acid sphingomyelinase deficiency (ASMD). Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":false,"slug":"e75.24-niemann-pick-disease"},{"code":"E75.240","title":"Niemann-Pick disease type A","description":"Niemann-Pick disease type A is a billable ICD-10-CM diagnosis code (E75.240). Inclusion terms: Acid sphingomyelinase deficiency type A (ASMD type A); Infantile neurovisceral acid sphingomyelinase deficiency. Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.240-niemann-pick-disease-type-a"},{"code":"E75.241","title":"Niemann-Pick disease type B","description":"Niemann-Pick disease type B is a billable ICD-10-CM diagnosis code (E75.241). Inclusion terms: Acid sphingomyelinase deficiency type B (ASMD type B); Chronic visceral acid sphingomyelinase deficiency. Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.241-niemann-pick-disease-type-b"},{"code":"E75.242","title":"Niemann-Pick disease type C","description":"Niemann-Pick disease type C is a billable ICD-10-CM diagnosis code (E75.242). Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.242-niemann-pick-disease-type-c"},{"code":"E75.243","title":"Niemann-Pick disease type D","description":"Niemann-Pick disease type D is a billable ICD-10-CM diagnosis code (E75.243). Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.243-niemann-pick-disease-type-d"},{"code":"E75.244","title":"Niemann-Pick disease type A/B","description":"Niemann-Pick disease type A/B is a billable ICD-10-CM diagnosis code (E75.244). Inclusion terms: Acid sphingomyelinase deficiency type A/B (ASMD type A/B); Chronic neurovisceral acid sphingomyelinase deficiency. Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.244-niemann-pick-disease-type-ab"},{"code":"E75.248","title":"Other Niemann-Pick disease","description":"Other Niemann-Pick disease is a billable ICD-10-CM diagnosis code (E75.248). Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.248-other-niemann-pick-disease"},{"code":"E75.249","title":"Niemann-Pick disease, unspecified","description":"Niemann-Pick disease, unspecified is a billable ICD-10-CM diagnosis code (E75.249). Inclusion terms: Acid sphingomyelinase deficiency (ASMD) NOS. Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.249-niemann-pick-disease-unspecified"},{"code":"E75.25","title":"Metachromatic leukodystrophy","description":"Metachromatic leukodystrophy is a billable ICD-10-CM diagnosis code (E75.25). Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.25-metachromatic-leukodystrophy"},{"code":"E75.26","title":"Sulfatase deficiency","description":"Sulfatase deficiency is a billable ICD-10-CM diagnosis code (E75.26). Inclusion terms: Multiple sulfatase deficiency (MSD). Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.26-sulfatase-deficiency"},{"code":"E75.27","title":"Pelizaeus-Merzbacher disease","description":"Pelizaeus-Merzbacher disease is a billable ICD-10-CM diagnosis code (E75.27). Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.27-pelizaeus-merzbacher-disease"},{"code":"E75.28","title":"Canavan disease","description":"Canavan disease is a billable ICD-10-CM diagnosis code (E75.28). Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.28-canavan-disease"},{"code":"E75.29","title":"Other sphingolipidosis","description":"Other sphingolipidosis is a billable ICD-10-CM diagnosis code (E75.29). Inclusion terms: Farber's syndrome; Sulfatide lipidosis. Excludes1 (not coded here): adrenoleukodystrophy [Addison-Schilder] (E71.528); mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.29-other-sphingolipidosis"},{"code":"E75.3","title":"Sphingolipidosis, unspecified","description":"Sphingolipidosis, unspecified is a billable ICD-10-CM diagnosis code (E75.3). Excludes1 (not coded here): mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.3-sphingolipidosis-unspecified"},{"code":"E75.4","title":"Neuronal ceroid lipofuscinosis","description":"Neuronal ceroid lipofuscinosis is a billable ICD-10-CM diagnosis code (E75.4). Inclusion terms: Batten disease; Bielschowsky-Jansky disease; Kufs disease; Spielmeyer-Vogt disease. Excludes1 (not coded here): mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.4-neuronal-ceroid-lipofuscinosis"},{"code":"E75.5","title":"Other lipid storage disorders","description":"Other lipid storage disorders is a billable ICD-10-CM diagnosis code (E75.5). Inclusion terms: Cerebrotendinous cholesterosis [van Bogaert-Scherer-Epstein]; Wolman's disease. Excludes1 (not coded here): mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.5-other-lipid-storage-disorders"},{"code":"E75.6","title":"Lipid storage disorder, unspecified","description":"Lipid storage disorder, unspecified is a billable ICD-10-CM diagnosis code (E75.6). Excludes1 (not coded here): mucolipidosis, types I-III (E77.0-E77.1); Refsum's disease (G60.1); 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). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e75.6-lipid-storage-disorder-unspecified"}],"hierarchy":[],"relatedCodes":[],"relevantCPTCodes":[],"documentationTips":[],"caseStudies":[],"description":"","overview":""}