E78.6
BillableLipoprotein deficiency
Lipoprotein deficiency
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Abetalipoproteinemia
- Depressed HDL cholesterol
- High-density lipoprotein deficiency
- Hypoalphalipoproteinemia
- Hypobetalipoproteinemia (familial)
- Lecithin cholesterol acyltransferase deficiency
- Tangier 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)
- sphingolipidosis (E75.0-E75.3)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Hereditary acanthocytosis11376001
- Alphalipoproteinaemia neuropathy15346004
- Alphalipoproteinemia neuropathy15346004
- Analphalipoproteinaemia15346004
- Analphalipoproteinemia15346004
- Analphaliproteinaemia15346004
- Analphaliproteinemia15346004
- Cholesterol thesaurismosis15346004
- Familial HDL deficiency15346004
- Familial high density lipoprotein deficiency15346004
- Familial hypoalphalipoproteinaemia15346004
- Familial hypoalphalipoproteinemia15346004
- Chorea acanthocytosis syndrome26848004
- Inborn error of lipoprotein metabolism43465001
- Familial lipoprotein deficiency49973006
- Familial hypobetalipoproteinaemia60193003
- Familial hypobetalipoproteinemia60193003
- Hypocholesteraemia61336008
- Hypocholesteremia61336008
- Hypocholesterolaemia61336008
- Hypocholesterolemia61336008
- Decreased lipoprotein124041005
- Lipoprotein below reference range124041005
- Hypoalphalipoproteinaemia190785000
- Hypoalphalipoproteinemia190785000
- Hypo-beta-lipoproteinaemia190786004
- Hypo-beta-lipoproteinemia190786004
- ABL - Abetalipoproteinaemia190787008
- ABL - Abetalipoproteinemia190787008
- Abetalipoproteinaemia190787008
- Abetalipoproteinemia190787008
- Apolipoprotein B deficiency190787008
- Bassen-Kornzweig disease190787008
- Homozygous familial hypobetalipoproteinaemia190787008
- Homozygous familial hypobetalipoproteinemia190787008
- Familial hypolipoproteinaemia238041007
- Familial hypolipoproteinemia238041007
- LCAT (lecithin-cholesterol acyltransferase) deficiency238091006
- LCAT deficiency238091006
- Lecithin cholesterol acyltransferase deficiency238091006
- FED - Fish-eye disease238092004
- Fish-eye disease238092004
- Partial LCAT (lecithin-cholesterol acyltransferase) deficiency238092004
- Partial LCAT deficiency238092004
- Familial hypobetalipoproteinaemia - homozygous form238093009
- Familial hypobetalipoproteinemia - homozygous form238093009
- Familial hypobetalipoproteinaemia - heterozygous form238094003
- Familial hypobetalipoproteinemia - heterozygous form238094003
- Apolipoprotein A-I deficiency238095002
- Apolipoprotein A-I variant disorder238096001
- Apo A-I Milano variant238097005
- Apo A-I Marburg variant238098000
- ApoA-I Munster variant 1238099008
- ApoA-I Munster variant 2238100000
- ApoA-I Munster variant 3238101001
- Apo A-I Giessen variant238102008
- Apo A-I variant fisheye-like syndrome238103003
- Acanthocytosis250249008
- Spiny prickle cells present250249008
- Lipoprotein deficiency disorder267436001
- Hypolipoproteinaemia363140000
- Hypolipoproteinemia363140000
- High density lipoprotein deficiency448834003
- Defective adenosine triphosphate-binding cassette transporter A1723579009
- Tangier disease723579009
- McLeod neuroacanthocytosis syndrome724172004
- X-linked McLeod syndrome724172004
- Ataxia co-occurrent and due to abetalipoproteinaemia724770001
- Ataxia co-occurrent and due to abetalipoproteinemia724770001
- Ataxia with abetalipoproteinaemia724770001
- Ataxia with abetalipoproteinemia724770001
- Autonomic neuropathy due to Tangier disease838348004
- High density lipoprotein below reference range1172654005
- Low density lipoprotein cholesterol below reference range1172655006
- Ophthalmoplegia due to abetalipoproteinaemia1208880009
- Ophthalmoplegia due to abetalipoproteinemia1208880009
- Complete LCAT (lecithin-cholesterol acyltransferase) deficiency1264565005
- Complete LCAT deficiency1264565005
- Familial lecithin cholesterol acyltransferase deficiency1264565005
- Norum disease1264565005
UMLS
- ABETALIPOPROTEINEMIAC0000744
- ABLC0000744
- ABL - AbetalipoproteinaemiaC0000744
- ABL - AbetalipoproteinemiaC0000744
- ACANTHOCYTOSISC0000744
- AbetalipoproteinaemiaC0000744
- AbetalipoproteinemiaC0000744
- Abetalipoproteinemia (disorder)C0000744
- AcanthocytosesC0000744
- AcanthocytosisC0000744
- BASSEN KORNZWEIG DISC0000744
- BASSEN-KORNZWEIG SYNDROMEC0000744
- Bassen Kornzweig DiseaseC0000744
- Bassen Kornzweig SyndromeC0000744
- Bassen Kornzweig syndromeC0000744
- Bassen-Kornzweig DiseaseC0000744
- Bassen-Kornzweig SyndromeC0000744
- Bassen-Kornzweig diseaseC0000744
- Bassen-Kornzweig syndromeC0000744
- Betalipoprotein Deficiency DiseaseC0000744
- Betalipoprotein Deficiency DiseasesC0000744
- Betalipoprotein deficiency diseaseC0000744
- Congenital betalipoprotein deficiency syndromeC0000744
- Deficiency Disease, BetalipoproteinC0000744
- Deficiency Diseases, BetalipoproteinC0000744
- Disease, Betalipoprotein DeficiencyC0000744
- Diseases, Betalipoprotein DeficiencyC0000744
- Homozygous familial hypobetalipoproteinaemiaC0000744
- Homozygous familial hypobetalipoproteinemiaC0000744
- MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN DEFICC0000744
- MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN DEFIC DISC0000744
- MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN DEFICIENCYC0000744
- MTP DEFICIENCYC0000744
- MTP deficiencyC0000744
- Microsomal Triglyceride Transfer Protein DeficiencyC0000744
- Microsomal Triglyceride Transfer Protein Deficiency DiseaseC0000744
- Microsomal triglyceride transfer protein deficiency diseaseC0000744
- abetalipoproteinemiaC0000744
- bassen kornzweig syndromeC0000744
- bassen-kornzweig diseaseC0000744
- bassen-kornzweig syndromeC0000744
- betalipoprotein deficiency diseaseC0000744
- microsomal triglyceride transfer protein deficiency diseaseC0000744
- ALPHA LCAT DEFICC0023195
- ALPHA LECITHIN CHOLESTEROL ACYLTRANSFERASE DEFICC0023195
- Acyltransferase Deficiency, Lecithin:CholesterolC0023195
- Alpha-LCAT deficiencyC0023195
- Alpha-lecithin:cholesterol acyltransferase deficiencyC0023195
- Complete LCAT (lecithin-cholesterol acyltransferase) deficiencyC0023195
- Complete LCAT deficiencyC0023195
- Deficiency, LCATC0023195
- Deficiency, alpha-LCATC0023195
- FLDC0023195
- Familial LCAT deficiencyC0023195
- Familial lecithin cholesterol acyltransferase deficiencyC0023195
- Familial lecithin cholesterol acyltransferase deficiency (disorder)C0023195
- Familial lecithin-cholesterol acyltransferase deficiencyC0023195
- LCAT DEFICC0023195
- LCAT DEFICIENCYC0023195
- LCAT DeficiencyC0023195
- LCAT deficiencyC0023195
- LCATA DeficienciesC0023195
- LCATA DeficiencyC0023195
- LCATA deficiencyC0023195
- LECITHIN CHOLESTEROL ACYLTRANSFERASE DEFICC0023195
- LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCYC0023195
- Lecithin Acyltransferase DeficiencyC0023195
- Lecithin Cholesterol Acyltransferase DeficiencyC0023195
- Lecithin acyltransferase deficiencyC0023195
- Lecithin cholesterol acyltransferase deficiencyC0023195
- Lecithin-cholesterol acyltransferase deficiencyC0023195
- Lecithin:Cholesterol Acyltransferase DeficiencyC0023195
- Lecithin:cholesterol acyltransferase deficiencyC0023195
- NORUM DISEASEC0023195
- Norum DiseaseC0023195
- Norum diseaseC0023195
- Norum's diseaseC0023195
- alpha LCAT DeficiencyC0023195
- alpha-LCAT DeficiencyC0023195
- alpha-Lecithin-Cholesterol Acyltransferase DeficiencyC0023195
- alpha-Lecithin:Cholesterol Acyltransferase DeficiencyC0023195
- familial cholesteryl ester deficiencyC0023195
- lcat deficiencyC0023195
- lecithin acyltransferase deficiencyC0023195
- lecithin cholesterol acyltransferase deficiencyC0023195
- norum diseaseC0023195
- ANALPHALIPOPROTEINEMIAC0039292
- Alpha High Density Lipoprotein Deficiency DiseaseC0039292
- Alpha high density lipoprotein deficiency diseaseC0039292
- AnalphalipoproteinaemiaC0039292
- AnalphalipoproteinemiaC0039292
- AnalphalipoproteinemiasC0039292
- AnalphaliproteinaemiaC0039292
- AnalphaliproteinemiaC0039292
- Cholesterol ThesaurismosesC0039292
- Cholesterol ThesaurismosisC0039292
- Cholesterol thesaurismosisC0039292
- Defective adenosine triphosphate-binding cassette transporter A1C0039292
- HDLDT1C0039292
- HIGH DENSITY LIPOPROTEIN DEFICIENCY, TANGIER TYPEC0039292
- HIGH DENSITY LIPOPROTEIN DEFICIENCY, TYPE 1C0039292
- High Density Lipoprotein Deficiency, Tangier TypeC0039292
- High Density Lipoprotein Deficiency, Type 1C0039292
- High Density Lipoprotein Deficiency, Type IC0039292
- High-Density Lipoprotein Deficiency, Tangier TypeC0039292
- High-Density Lipoprotein Deficiency, Type IC0039292
- TANGIER DISC0039292
- TANGIER DISEASEC0039292
- TGDC0039292
- Tangier DiseaseC0039292
- Tangier diseaseC0039292
- Tangier disease (disorder)C0039292
- Thesaurismoses, CholesterolC0039292
- Thesaurismosis, CholesterolC0039292
- alpha lipoprotein deficiencyC0039292
- disease tangiersC0039292
- diseases tangiersC0039292
- tangier diseaseC0039292
- Depressed HDL cholesterolC2874290
- FHBLC1862596
- Familial HypobetalipoproteinemiaC1862596
- Familial hypobetalipoproteinaemiaC1862596
- Familial hypobetalipoproteinemiaC1862596
- Familial hypobetalipoproteinemia (disorder)C1862596
- HYPOBETALIPOPROTEINEMIA, FAMILIALC1862596
- Hypo beta LipoproteinemiaC1862596
- Hypo beta LipoproteinemiasC1862596
- HypobetalipoproteinemiaC1862596
- Hypobetalipoproteinemia (familial)C1862596
- HypobetalipoproteinemiasC1862596
- HDL Cholesterol, Low SerumC0473527
- Hypo alpha LipoproteinemiaC0473527
- Hypo alpha LipoproteinemiasC0473527
- HypoalphalipoproteinaemiaC0473527
- HypoalphalipoproteinemiaC0473527
- Hypoalphalipoproteinemia (disorder)C0473527
- HypoalphalipoproteinemiasC0473527
- Lipoproteinemia, Hypo alphaC0473527
- Lipoproteinemias, Hypo alphaC0473527
- alpha Lipoproteinemia, HypoC0473527
- High density lipoprotein deficiencyC3165209
- High density lipoprotein deficiency (disorder)C3165209
- High-density lipoprotein deficiencyC3165209
- HypolipoproteinaemiaC0020623
- HypolipoproteinemiaC0020623
- Hypolipoproteinemia (disorder)C0020623
- HypolipoproteinemiasC0020623
- Lack of fat in bloodC0020623
- Lipoprotein deficiencyC0020623
- Lipoprotein deficiency disorderC0020623
- Lipoprotein deficiency disorder (disorder)C0020623
- deficiency lipoproteinC0020623
- hypolipoproteinemiaC0020623
- lipoprotein deficiencyC0020623
Frequently Asked Questions
What is ICD-10 code E78.6?
ICD-10-CM code E78.6 represents "Lipoprotein deficiency". It is a billable/specific code that can be used on a claim.
Is E78.6 a billable code?
Yes, E78.6 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E78.6 in?
E78.6 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E78.6?
E78.6 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 4 more.
What SNOMED CT codes does E78.6 map to?
E78.6 maps to 37 SNOMED CT concepts: 190787008, 250249008, 15346004, 238102008, 238098000, and 32 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E78.6?
E78.6 is linked to 8 UMLS Concept Unique Identifiers: C0000744, C0023195, C0039292, C2874290, C1862596, and 3 more. 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.