E78.89
BillableOther lipoprotein metabolism disorders
Other lipoprotein metabolism disorders
Coding Notes
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
- Lipofuscinosis14210003
- Lobular panniculitis20196005
- Brown bowel syndrome28212002
- Intestinal lipofuscinosis28212002
- Hyalinosis cutis et mucosae38692000
- Lipid proteinosis38692000
- Lipoid proteinosis38692000
- Lipoidosis cutis et mucosae38692000
- Urbach-Wiethe disease38692000
- Lipogranulomatosis subcutanea of Rothmann and Makai51696001
- Rothmann-Makai syndrome51696001
- Subcutaneous lipogranulomatosis51696001
- Familial disease with storage of sterols (other than cholesterol)58618005
- Proteinosis59714007
- Acid ceramidase deficiency79935000
- Acylsphingosine deacylase deficiency79935000
- Ceramidase deficiency79935000
- Disseminated lipogranulomatosis79935000
- Farber disease79935000
- Farber lipogranulomatosis79935000
- Farber's disease79935000
- Farber's lipogranulomatosis79935000
- Farber-Uzman syndrome79935000
- Increased lipoprotein124040006
- Lipoprotein above reference range124040006
- Decreased lipoprotein124041005
- Lipoprotein below reference range124041005
- Deficiency of glycerophosphocholine phosphodiesterase124444008
- Hypolipidaemia238090007
- Hypolipidemia238090007
- Sitosterolaemia238104009
- Sitosterolemia238104009
- Finding of triglyceride level365795001
- Triglyceride level365795001
- Triglyceride level - finding365795001
- Dyslipidaemia370992007
- Dyslipidemia370992007
- Fat overload syndrome426020004
- Homozygous sitosterolaemia428014009
- Homozygous sitosterolemia428014009
- Heterozygous sitosterolaemia428530009
- Heterozygous sitosterolemia428530009
- LDLR (low density lipoprotein receptor) mutation445010006
- Low density lipoprotein receptor mutation445010006
- Low density lipoprotein cholesterol above reference range445445006
- Raised low density lipoprotein cholesterol445445006
- LAL (Lysosomal acid lipase) deficiency715923003
- LALD - Lysosomal acid lipase deficiency715923003
- Lysosomal acid lipase deficiency715923003
- Hepatic lipase deficiency720940008
- Hyperlipidaemia due to hepatic triglyceride lipase deficiency720940008
- Hyperlipidemia due to hepatic triglyceride lipase deficiency720940008
- Amish infantile epilepsy syndrome722762005
- GM3 synthase deficiency722762005
- Ganglioside GM3 synthase deficiency722762005
- Infantile-onset symptomatic epilepsy syndrome722762005
- Combined pancreatic lipase and colipase deficiency763212006
- LDLRAP1 (Low density lipoprotein receptor adaptor protein 1) mutation767134003
- Low density lipoprotein receptor adaptor protein 1 mutation767134003
- Combined heterozygous low density lipoprotein receptor co-occurrent with low density lipoprotein receptor adaptor protein 1 mutations767139008
- MEND (male emopamil-binding protein disorder with neurological defect) syndrome782739000
- Male EBP (emopamil-binding protein) disorder with neurological defect782739000
- Male emopamil-binding protein disorder with neurological defect782739000
- High density lipoprotein below reference range1172654005
- Diabetic dyslipidemia associated with type 2 diabetes mellitus761000119102
- Dyslipidemia associated with type II diabetes mellitus761000119102
- Dyslipidemia due to type 2 diabetes mellitus761000119102
- Dyslipidemia with high density lipoprotein below reference range and triglyceride above reference range due to type 2 diabetes mellitus111231000119109
Frequently Asked Questions
What is the ICD-10 code for other lipoprotein metabolism disorders?
The ICD-10-CM code for other lipoprotein metabolism disorders is E78.89. The full clinical description is "Other lipoprotein metabolism disorders". E78.89 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E78.89 mean?
ICD-10-CM code E78.89 represents "Other lipoprotein metabolism 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 E78.89 a billable code?
Yes, E78.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E78.89 in?
E78.89 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E78.89?
E78.89 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 E78.89 map to?
E78.89 maps to 30 SNOMED CT concepts: 79935000, 722762005, 28212002, 767139008, 763212006, and 25 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E78.89?
E78.89 is linked to 1 UMLS Concept Unique Identifier: C0348495. 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.