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 newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- •mucolipidosis, types I-IIIE77.0-E77.1
- •Refsum's diseaseG60.1
Related Codes(6)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(235)
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
Clinical Terms
- Disorder of cholesterol metabolism
- Familial disease with storage of sterols (other than cholesterol)
- Ichthyosiform erythroderma with leukocyte vacuolation
- Deficiencies, Acid Lipase
- Sitosterolaemia with xanthomatosis
- Beta-sitosterolaemia
- Disorder of lipid storage and metabolism
- Adult sialic acid storage disease
- Lipid storage myopathy AND congenital ichthyosis
- van Bogaert-Scherer-Epstein syndrome
- Xanthoma due to lipid storage disease
- LIPA Deficiencies
- LYSOSOMAL ACID LIPASE DEFICIENCY, COMPLETE
- Acid lipase deficiency
- Bile acid synthesis disorder
- Van Bogaert-Scherer-Epstein disease
- Familial Xanthomatosis
- Wolmans Disease
- Deficiencies, LAL
- Lipid storage myopathy
- Bile acid synthetic defect
- Deficiency of cholesterol esterase AND triacylglycerol lipase
- Inborn error of bile acid synthesis
- Deficiency, LAL
- Sitosterolemic xanthomatosis
- Disorder of sialic acid metabolism
- Tendinous xanthoma
- beta-Sitosterolemia
- CHOLESTEROL ESTER HYDROLASE DEFICIENCY, COMPLETE
- Sitosterolemia with xanthomatosis
- Chemically-induced lipidosis
- LIPA DEFICIENCY, COMPLETE
- Pulmonary xanthoma
- LIPA Deficiency
- Wolman disease
- Cerebral cholesterinosis
- Xanthoma due to abnormality of lipid metabolism
- LALD - Lysosomal acid lipase deficiency
- Neutral lipid storage disease without ichthyosis
- Xanthomatosis, Wolmans
- Wolman's Disease
- Papular xanthoma
- Xanthomatoses, Familial
- Disorder of bile acid synthesis
- Wolman's Xanthomatosis
- Xanthomatosis, Wolman's
- Wolman's disease (disorder)
- Xanthoma tendinosum
- Xanthoma of lung
- Wolman Disease with Hypolipoproteinemia and Acanthocytosis
- Disease, Wolman
- Chanarin-Miranda syndrome
- LAL Deficiency
- BASD - Bile acid synthetic defect
- Sitosterolaemic xanthomatosis
- Acid esterase deficiency
- LYSOSOMAL ACID LIPASE DEFICIENCY, ACUTE INFANTILE
- Acid Lipase Deficiencies
- Familial Xanthomatoses
- Deficiencies, LIPA
- Primary familial xanthomatosis with adrenal calcification
- Lipase Deficiency, Acid
- Primary triglyceride deposit cardiomyovasculopathy
- Primary familial xanthomatosis
- Salla disease
- Cholestanol storage disease
- Lipase Deficiencies, Acid
- Ichthyotic neutral lipid storage disease
- Lysosomal acid lipase deficiency
- Xanthomatosis, Familial
- Pulmonary lipid storage disease
- Cerebrotendinous cholesterosis [van Bogaert-Scherer-Epstein]
- Sitosterolaemia
- WOLD
- Sialic storage disease
- Disorder of cholesterol catabolism
- Wolman xanthomatosis
- WOLMAN DIS
- Chemically induced lipidosis
- Ichthyosiform erythroderma with leucocyte vacuolation
- Liposomal Acid Lipase Deficiency, Wolman Type
- CTX - Cerebrotendinous xanthomatosis
- Neutral lipid storage disease
- CESD - Cholesterol ester storage disease
- Cholesterol ester hydrolase deficiency
- Synthetic defect of bile acids
- Deficiency, LIPA
- Ataxia due to cerebrotendinous xanthomatosis
- Sialuria, Finnish type
- Disease, Wolman's
- Familial visceral xanthomatosis
- LAL Deficiencies
- Xanthomatosis, Wolman
- Cholestanolosis
- LAL DEFICIENCY, COMPLETE
- Triglyceride storage disease with ichthyosis
- Deficiency, Acid Lipase
- Acid Cholesteryl Ester Hydrolase Deficiency, Wolman Type
- WOLMANS DIS
- Sitosterolemia
- Neutral lipid storage disease with myopathy
- LAL (Lysosomal acid lipase) deficiency
- Neutral lipid storage disease with severe cardiovascular involvement
- Chanarin-Dorfman disease
- Cerebrotendinous xanthomatosis
- Cholesterol ester storage disease
- Cerebrotendinous cholesterinosis
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.
How does E75.5 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other lipid storage disorders affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of E75.5?
E75.5 maps to the ICD-11 code: 5C52.Z (Inborn errors of lipid metabolism, unspecified).
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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.