E85.2
BillableHeredofamilial amyloidosis, unspecified
Heredofamilial amyloidosis, unspecified
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(6)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(125)
SNOMED CT
- Amyloid nephropathy with deafness and urticaria15123008
- Familial amyloid nephropathy with urticaria AND deafness15123008
- Muckle-Wells syndrome15123008
- Muckle-Wells type amyloidosis15123008
- Amyloid nephropathy48713002
- Lardaceous kidney48713002
- Nephropathic amyloidosis48713002
- Renal amyloidosis48713002
- Soapy kidney48713002
- Waxy kidney48713002
- Amyloid nephropathy of Ostertag66451004
- Amyloidosis VIII66451004
- Familial renal amyloidosis66451004
- Familial visceral amyloidosis, Ostertag type66451004
- German type amyloidosis66451004
- Amyloid myopathy193247000
- CAA - Cerebral amyloid angiopathy230724001
- Cerebral amyloid angiopathy230724001
- Congophilic angiopathy230724001
- Hereditary cerebrovascular amyloidosis237867001
- Familial non-neuropathic amyloidosis237868006
- Nonneuropathic heredofamilial amyloidosis237868006
- Localised hereditary amyloidosis237869003
- Localized hereditary amyloidosis237869003
- Organ limited hereditary amyloidosis237869003
- Familial lichen amyloidosis237870002
- Primary familial amyloid myopathy237873000
- Heredofamilial systemic amyloidosis affecting skin402459005
- Familial localised cutaneous amyloidosis402463003
- Familial localized cutaneous amyloidosis402463003
- Systemic amyloidosis affecting skin402719006
- Cryopyrin associated periodic syndrome430079001
- Autosomal dominant beta2-microglobulinic amyloidosis722292000
- Variant ABeta2M amyloidosis722292000
- Chronic diarrhea with hereditary sensory and autonomic neuropathy733422008
- Chronic diarrhoea with hereditary sensory and autonomic neuropathy733422008
- PrP (prion protein) systemic amyloidosis733422008
- Prion protein systemic amyloidosis733422008
- Primary localised cutaneous amyloidosis733729003
- Primary localized cutaneous amyloidosis733729003
- AGel amyloidosis783160006
- Familial amyloid polyneuropathy type IV783160006
- Familial amyloidosis Finnish type783160006
- Gelsolin amyloidosis783160006
- Hereditary amyloidosis Finnish type783160006
- Hereditary gelsolin amyloidosis783160006
- Lattice corneal dystrophy type II783160006
- ABri amyloidosis783161005
- Familial British dementia with amyloid angiopathy783161005
- Familial dementia British type783161005
- ADan amyloidosis783258000
- Familial dementia Danish type783258000
- ITM2B amyloidosis1187126002
- ITM2B-related amyloidosis1187126002
- ITM2B-related cerebral amyloid angiopathy1187126002
- Integral membrane protein 2B related amyloidosis1187126002
- Localised hereditary amyloidosis of heart1187149000
- Localised hereditary cardiac amyloidosis1187149000
- Localized hereditary amyloidosis of heart1187149000
- Localized hereditary cardiac amyloidosis1187149000
- Hereditary amyloidosis367601000119103
- Hereditary systemic amyloidosis107311000119104
Clinical Terms
- Localized hereditary cardiac amyloidosis
- Primary familial amyloid myopathy
- Hereditary gelsolin amyloidosis
- Familial dementia British type
- Familial dementia Danish type
- ITM2B amyloidosis
- Amyloidosis VIII
- Localized hereditary amyloidosis
- Lattice corneal dystrophy type II
- AGel amyloidosis
- Hereditary systemic amyloidosis
- CAA - Cerebral amyloid angiopathy
- Muckle-Wells syndrome
- Localized hereditary amyloidosis of heart
- Nephropathic amyloidosis
- Primary localized cutaneous amyloidosis
- Renal amyloidosis
- Heredofamilial systemic amyloidosis affecting skin
- Autosomal dominant beta2-microglobulinic amyloidosis
- Localised hereditary amyloidosis
- Localised hereditary amyloidosis of heart
- Localised hereditary cardiac amyloidosis
- Systemic amyloidosis affecting skin
- ITM2B-related cerebral amyloid angiopathy
- Familial localised cutaneous amyloidosis
- ABri amyloidosis
- Chronic diarrhea with hereditary sensory and autonomic neuropathy
- Familial amyloid nephropathy with urticaria AND deafness
- Familial visceral amyloidosis, Ostertag type
- Waxy kidney
- Familial renal amyloidosis
- Hereditary amyloidosis Finnish type
- Lardaceous kidney
- Amyloid nephropathy
- Prion protein systemic amyloidosis
- Gelsolin amyloidosis
- Cryopyrin associated periodic syndrome
- Familial amyloid polyneuropathy type IV
- Amyloid myopathy
- Variant ABeta2M amyloidosis
- Integral membrane protein 2B related amyloidosis
- Cerebral amyloid angiopathy
- Amyloid nephropathy with deafness and urticaria
- Primary localised cutaneous amyloidosis
- ADan amyloidosis
- Muckle-Wells type amyloidosis
- Hereditary cerebrovascular amyloidosis
- Familial localized cutaneous amyloidosis
- Congophilic angiopathy
- Amyloid nephropathy of Ostertag
- Organ limited hereditary amyloidosis
- Familial British dementia with amyloid angiopathy
- German type amyloidosis
- Nonneuropathic heredofamilial amyloidosis
- PrP (prion protein) systemic amyloidosis
- ITM2B-related amyloidosis
- Soapy kidney
- Hereditary amyloidosis
- Chronic diarrhoea with hereditary sensory and autonomic neuropathy
- Familial lichen amyloidosis
- Familial amyloidosis Finnish type
- Familial non-neuropathic amyloidosis
Frequently Asked Questions
What is the ICD-10 code for heredofamilial amyloidosis, unspecified?
The ICD-10-CM code for heredofamilial amyloidosis, unspecified is E85.2. The full clinical description is "Heredofamilial amyloidosis, unspecified". E85.2 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E85.2 mean?
ICD-10-CM code E85.2 represents “Heredofamilial amyloidosis, unspecified”. 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 E85.2 a billable code?
Yes, E85.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E85.2 in?
E85.2 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E85.2?
E85.2 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 3 more.
What SNOMED CT codes does E85.2 map to?
E85.2 maps to 24 SNOMED CT concepts: 783161005, 783258000, 783160006, 193247000, 48713002, and 19 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E85.2?
E85.2 is linked to 1 UMLS Concept Unique Identifier: C0348506. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E85.2 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like heredofamilial amyloidosis, unspecified 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 E85.2?
E85.2 maps to the ICD-11 code: 5D00.2Z (Hereditary amyloidosis, 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.