E85.2
BillableHeredofamilial amyloidosis, unspecified
Heredofamilial amyloidosis, unspecified
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Also Known As / Clinical Terms
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
Frequently Asked Questions
What is ICD-10 code E85.2?
ICD-10-CM code E85.2 represents "Heredofamilial amyloidosis, unspecified". It 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.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.