E75.5
BillableOther lipid storage disorders
Other lipid storage disorders
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Cerebrotendinous cholesterosis [van Bogaert-Scherer-Epstein]
- Wolman's disease
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
- Chanarin-Dorfman disease19604005
- Chanarin-Miranda syndrome19604005
- Ichthyosiform erythroderma with leucocyte vacuolation19604005
- Ichthyosiform erythroderma with leukocyte vacuolation19604005
- Ichthyotic neutral lipid storage disease19604005
- Lipid storage myopathy AND congenital ichthyosis19604005
- Neutral lipid storage disease19604005
- Triglyceride storage disease with ichthyosis19604005
- CESD - Cholesterol ester storage disease57218003
- Cholesterol ester storage disease57218003
- Familial disease with storage of sterols (other than cholesterol)58618005
- CTX - Cerebrotendinous xanthomatosis63246000
- Cerebral cholesterinosis63246000
- Cerebrotendinous cholesterinosis63246000
- Cerebrotendinous xanthomatosis63246000
- Cholestanol storage disease63246000
- Cholestanolosis63246000
- Van Bogaert-Scherer-Epstein disease63246000
- van Bogaert-Scherer-Epstein syndrome63246000
- Beta-sitosterolaemia65419005
- Sitosterolaemia with xanthomatosis65419005
- Sitosterolaemic xanthomatosis65419005
- Sitosterolemia with xanthomatosis65419005
- Sitosterolemic xanthomatosis65419005
- beta-Sitosterolemia65419005
- Tendinous xanthoma69880002
- Xanthoma tendinosum69880002
- Acid esterase deficiency82500001
- Acid lipase deficiency82500001
- Deficiency of cholesterol esterase AND triacylglycerol lipase82500001
- Familial visceral xanthomatosis82500001
- Primary familial xanthomatosis82500001
- Primary familial xanthomatosis with adrenal calcification82500001
- Wolman disease82500001
- Wolman xanthomatosis82500001
- Wolman's disease82500001
- Adult sialic acid storage disease87074006
- Salla disease87074006
- Sialuria, Finnish type87074006
- Chemically induced lipidosis111382002
- Chemically-induced lipidosis111382002
- Disorder of cholesterol metabolism123963007
- Pulmonary lipid storage disease233720006
- BASD - Bile acid synthetic defect235915002
- Bile acid synthesis disorder235915002
- Bile acid synthetic defect235915002
- Disorder of bile acid synthesis235915002
- Inborn error of bile acid synthesis235915002
- Synthetic defect of bile acids235915002
- Disorder of lipid storage and metabolism238017009
- Disorder of cholesterol catabolism238032002
- Disorder of sialic acid metabolism238050009
- Sitosterolaemia238104009
- Sitosterolemia238104009
- Lipid storage myopathy240095001
- Sialic storage disease278991002
- Xanthoma due to abnormality of lipid metabolism402724009
- Neutral lipid storage disease with myopathy699315005
- Neutral lipid storage disease without ichthyosis699315005
- Pulmonary xanthoma707364007
- Xanthoma of lung707364007
- LAL (Lysosomal acid lipase) deficiency715923003
- LALD - Lysosomal acid lipase deficiency715923003
- Lysosomal acid lipase deficiency715923003
- Papular xanthoma765221009
- Ataxia due to cerebrotendinous xanthomatosis1155955003
- Xanthoma due to lipid storage disease1256077007
- Neutral lipid storage disease with severe cardiovascular involvement1279844009
- Primary triglyceride deposit cardiomyovasculopathy1279844009
UMLS
- Acid Cholesteryl Ester Hydrolase Deficiency, Wolman TypeC0043208
- Acid Lipase DeficienciesC0043208
- Acid Lipase DeficiencyC0043208
- Acid esterase deficiencyC0043208
- Acid lipase deficiencyC0043208
- CHOLESTEROL ESTER HYDROLASE DEFICIENCY, COMPLETEC0043208
- Cholesterol ester hydrolase deficiencyC0043208
- Deficiencies, Acid LipaseC0043208
- Deficiencies, LALC0043208
- Deficiencies, LIPAC0043208
- Deficiency of cholesterol esterase AND triacylglycerol lipaseC0043208
- Deficiency, Acid LipaseC0043208
- Deficiency, LALC0043208
- Deficiency, LIPAC0043208
- Disease, WolmanC0043208
- Disease, Wolman'sC0043208
- Familial XanthomatosesC0043208
- Familial XanthomatosisC0043208
- Familial visceral xanthomatosisC0043208
- Familial xanthomatosisC0043208
- LAL DEFICIENCY, COMPLETEC0043208
- LAL DeficienciesC0043208
- LAL DeficiencyC0043208
- LIPA DEFICIENCY, COMPLETEC0043208
- LIPA DeficienciesC0043208
- LIPA DeficiencyC0043208
- LIPA deficiencyC0043208
- LYSOSOMAL ACID LIPASE DEFICIENCY, ACUTE INFANTILEC0043208
- LYSOSOMAL ACID LIPASE DEFICIENCY, COMPLETEC0043208
- Lipase Deficiencies, AcidC0043208
- Lipase Deficiency, AcidC0043208
- Liposomal Acid Lipase Deficiency, Wolman TypeC0043208
- Lysosomal Acid Lipase DeficiencyC0043208
- Primary familial xanthomatosisC0043208
- Primary familial xanthomatosis with adrenal calcificationC0043208
- WOLDC0043208
- WOLMAN DISC0043208
- WOLMAN DISEASEC0043208
- WOLMANS DISC0043208
- Wolman DiseaseC0043208
- Wolman Disease with Hypolipoproteinemia and AcanthocytosisC0043208
- Wolman diseaseC0043208
- Wolman xanthomatosisC0043208
- Wolman's DiseaseC0043208
- Wolman's XanthomatosisC0043208
- Wolman's diseaseC0043208
- Wolman's disease (disorder)C0043208
- Wolmans DiseaseC0043208
- Xanthomatoses, FamilialC0043208
- Xanthomatosis, FamilialC0043208
- Xanthomatosis, WolmanC0043208
- Xanthomatosis, Wolman'sC0043208
- Xanthomatosis, WolmansC0043208
- acid lipase deficiencyC0043208
- wolman diseaseC0043208
- wolman's diseaseC0043208
- wolmans diseaseC0043208
- Cerebrotendinous cholesterosis [van Bogaert-Scherer-Epstein]C2874275
- Other lipid storage disordersC0348490
Frequently Asked Questions
What is the ICD-10 code for other lipid storage disorders?
The ICD-10-CM code for other lipid storage disorders is E75.5. The full clinical description is "Other lipid storage disorders". E75.5 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E75.5 mean?
ICD-10-CM code E75.5 represents "Other lipid storage disorders". 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 E75.5 a billable code?
Yes, E75.5 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E75.5 in?
E75.5 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E75.5?
E75.5 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 E75.5 map to?
E75.5 maps to 26 SNOMED CT concepts: 82500001, 87074006, 1155955003, 235915002, 65419005, and 21 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E75.5?
E75.5 is linked to 3 UMLS Concept Unique Identifiers: C0043208, C2874275, C0348490. 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.