AutoICD API

E78.89

Billable

Other lipoprotein metabolism disorders

Other lipoprotein metabolism disorders

Status

Billable / Specific

Block

E70-E88

Parent Code

E78.8

Coding Notes

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(1)
E78.81

Lipoid dermatoarthritis

Billable

Related Conditions

Hyperlipidemia
Also Known As / Clinical Terms(139)

SNOMED CT

UMLS

Clinical Terms

  • Familial disease with storage of sterols (other than cholesterol)
  • Other disorders of lipoprotein metabolism
  • Lysosomal acid lipase deficiency
  • Low density lipoprotein receptor adaptor protein 1 mutation
  • LALD - Lysosomal acid lipase deficiency
  • Ganglioside GM3 synthase deficiency
  • Lipid proteinosis
  • Low density lipoprotein cholesterol above reference range
  • Hypolipidaemia
  • Male EBP (emopamil-binding protein) disorder with neurological defect
  • Sitosterolaemia
  • Ceramidase deficiency
  • Heterozygous sitosterolemia
  • Triglyceride level
  • Amish infantile epilepsy syndrome
  • Combined pancreatic lipase and colipase deficiency
  • Subcutaneous lipogranulomatosis
  • Finding of triglyceride level
  • Dyslipidaemia
  • Proteinosis
  • Farber's disease
  • Heterozygous sitosterolaemia
  • High density lipoprotein below reference range
  • Dyslipidemia due to type 2 diabetes mellitus
  • Hypolipidemia
  • Acylsphingosine deacylase deficiency
  • Infantile-onset symptomatic epilepsy syndrome
  • Deficiency of glycerophosphocholine phosphodiesterase
  • Decreased lipoprotein
  • Lipoprotein above reference range
  • LDLR (low density lipoprotein receptor) mutation
  • Farber disease
  • Combined heterozygous low density lipoprotein receptor co-occurrent with low density lipoprotein receptor adaptor protein 1 mutations
  • Intestinal lipofuscinosis
  • Sitosterolemia
  • Lipoprotein below reference range
  • Disseminated lipogranulomatosis
  • Dyslipidemia with high density lipoprotein below reference range and triglyceride above reference range due to type 2 diabetes mellitus
  • Lipofuscinosis
  • Homozygous sitosterolaemia
  • Hyalinosis cutis et mucosae
  • Raised low density lipoprotein cholesterol
  • Dyslipidemia
  • Hyperlipidaemia due to hepatic triglyceride lipase deficiency
  • Urbach-Wiethe disease
  • Dyslipidemia associated with type II diabetes mellitus
  • Lobular panniculitis
  • MEND (male emopamil-binding protein disorder with neurological defect) syndrome
  • LAL (Lysosomal acid lipase) deficiency
  • Triglyceride level - finding
  • Brown bowel syndrome
  • Increased lipoprotein
  • GM3 synthase deficiency
  • Hepatic lipase deficiency
  • Farber lipogranulomatosis
  • Farber-Uzman syndrome
  • Hyperlipidemia due to hepatic triglyceride lipase deficiency
  • Low density lipoprotein receptor mutation
  • Fat overload syndrome
  • Lipoidosis cutis et mucosae
  • LDLRAP1 (Low density lipoprotein receptor adaptor protein 1) mutation
  • Male emopamil-binding protein disorder with neurological defect
  • Lipoid proteinosis
  • Lipogranulomatosis subcutanea of Rothmann and Makai
  • Diabetic dyslipidemia associated with type 2 diabetes mellitus
  • Rothmann-Makai syndrome
  • Homozygous sitosterolemia
  • Acid ceramidase deficiency
  • Farber's lipogranulomatosis
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.

How does E78.89 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other lipoprotein metabolism 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 E78.89?

There is no direct ICD-11 mapping available for E78.89 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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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.