E85.4
BillableOrgan-limited amyloidosis
Organ-limited amyloidosis
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Localized amyloidosis
- Transthyretin-related (ATTR) familial amyloid cardiomyopathy
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Also Known As / Clinical Terms
SNOMED CT
- AS beta protein amyloidosis4645000
- Senile brain amyloidosis4645000
- Ocular amyloid deposit8231007
- Hepatic amyloidosis9551004
- Gingival amyloidosis11426004
- AS transthyretin amyloidosis16573007
- Amyloid heart muscle disease16573007
- Cardiac amyloidosis16573007
- Senile cardiac amyloidosis16573007
- Stiff heart syndrome16573007
- Wild-type transthyretin cardiac amyloidosis16573007
- Danish type amyloidosis27097002
- Danish type familial amyloid cardiomyopathy27097002
- Denmark type amyloidosis27097002
- Familial amyloid cardiomyopathy27097002
- Familial amyloid heart disease27097002
- Familial cardiomyopathy35728003
- Primary familial cardiomyopathy35728003
- Bullous cutaneous amyloid38606009
- Bullous cutaneous amyloidosis38606009
- Isolated atrial amyloid39502009
- Isolated corneal amyloidosis40933005
- AF type amyloidosis42295001
- Familial amyloid polyneuropathy42295001
- Familial neuropathic amyloidosis42295001
- Familial polyneuropathic amyloidosis42295001
- Neuropathic heredofamilial amyloidosis42295001
- Amyloidosis VII43532007
- Familial oculoleptomeningeal amyloidosis43532007
- Hereditary oculoleptomeningeal amyloid angiopathy43532007
- Ohio type amyloidosis43532007
- Amyloid nephropathy48713002
- Lardaceous kidney48713002
- Nephropathic amyloidosis48713002
- Renal amyloidosis48713002
- Soapy kidney48713002
- Waxy kidney48713002
- Dutch type amyloidosis56453003
- Hereditary cerebral amyloid angiopathy, Dutch type56453003
- Hereditary cerebral haemorrhage with amyloidosis - Dutch type56453003
- Hereditary cerebral hemorrhage with amyloidosis - Dutch type56453003
- Localised amyloidosis56871000
- Localized amyloidosis56871000
- Conjunctival amyloidosis59017008
- AS type amyloidosis69078007
- Age-related amyloidosis69078007
- Senile amyloidosis69078007
- Macular cutaneous amyloidosis111032003
- Amyloidosis IX111390002
- Dominant primary localised cutaneous amyloidosis111390002
- Dominant primary localized cutaneous amyloidosis111390002
- Familial amyloidosis cutis111390002
- Familial generalised dyschromic amyloidosis cutis111390002
- Familial generalized dyschromic amyloidosis cutis111390002
- Autonomic neuropathy due to amyloidosis192918007
- Pulmonary amyloidosis196135008
- Amyloidosis of skin201337008
- Neuropathy associated with dysproteinaemias230585004
- Neuropathy associated with dysproteinemias230585004
- CAA - Cerebral amyloid angiopathy230724001
- Cerebral amyloid angiopathy230724001
- Congophilic angiopathy230724001
- Sporadic cerebral amyloid angiopathy230725000
- Amyloid of cornea231928002
- Corneal amyloidosis231928002
- Amyloid of vitreous232076001
- Vitreous amyloid232076001
- Laryngeal amyloidosis232459006
- Amyloidosis of spleen234510005
- Arthritis due to beta-2 microglobulin amyloidosis236543006
- Arthritis due to haemodialysis-associated amyloidosis236543006
- Arthritis due to hemodialysis-associated amyloidosis236543006
- Beta-2 microglobulin arthropathy236543006
- Hereditary cerebrovascular amyloidosis237867001
- Familial non-neuropathic amyloidosis237868006
- Nonneuropathic heredofamilial amyloidosis237868006
- Localised hereditary amyloidosis237869003
- Localized hereditary amyloidosis237869003
- Organ limited hereditary amyloidosis237869003
- Poikilodermal cutaneous amyloid237872005
- Localised non-hereditary amyloidosis237875007
- Localized non-hereditary amyloidosis237875007
- Organ limited non-hereditary amyloidosis237875007
- Amyloid arthritis237876008
- Amyloid arthropathy237876008
- Arthritis secondary to amyloidosis237876008
- Arthropathy in amyloidosis237876008
- Articular amyloid237876008
- Deposit on gingivae249411008
- Amyloid of bladder278899001
- Amyloid of urinary bladder278899001
- Amyloid of prostate282354001
- Amyloid of testes282355000
- Testicular amyloid282355000
- Amyloid of ureter282357008
- Amyloid disease of the urethra311495006
- Macroglossia due to amyloidosis402455004
- Heredofamilial systemic amyloidosis affecting skin402459005
- Familial amyloid polyneuropathy affecting skin402460000
- Familial amyloid polyneuropathy with cutaneous amyloidosis402460000
- Secondary localised cutaneous amyloidosis402464009
- Secondary localized cutaneous amyloidosis402464009
- Systemic amyloidosis affecting skin402719006
- Amyloidosis limited to skin402720000
- Nodular amyloidosis716704007
- PLCNA - Primary localised cutaneous nodular amyloidosis716704007
- PLCNA - Primary localized cutaneous nodular amyloidosis716704007
- Primary localised cutaneous nodular amyloidosis716704007
- Primary localized cutaneous nodular amyloidosis716704007
- Amyloid lichen718105008
- Lichen amyloidosis718105008
- Lichen amyloidosus718105008
- Amyloidosis of small intestine721661009
- HCHWA - hereditary cerebral haemorrhage with amyloidosis724357007
- HCHWA - hereditary cerebral hemorrhage with amyloidosis724357007
- Hereditary cerebral haemorrhage with amyloidosis724357007
- Hereditary cerebral hemorrhage with amyloidosis724357007
- Primary localised cutaneous amyloidosis733729003
- Primary localized cutaneous amyloidosis733729003
- Acquired abnormality of atrium735569003
- Acquired atrial abnormality735569003
- Amyloidosis cutis dyschromia764849002
- Amyloidosis cutis dyschromica764849002
- Macule of skin829994007
- Infiltrative cardiomyopathy871646007
- Cardiac familial non-neuropathic amyloidosis1187147003
- Familial non-neuropathic amyloidosis of heart1187147003
- Disorder of glomerulus due to organ-limited amyloidosis1187555004
- Glomerular disorder due to organ-limited amyloidosis1187555004
- Disorder of glomerulus due to amyloidosis1187557007
- Glomerular disorder due to amyloidosis1187557007
Frequently Asked Questions
What is the ICD-10 code for organ-limited amyloidosis?
The ICD-10-CM code for organ-limited amyloidosis is E85.4. The full clinical description is "Organ-limited amyloidosis". E85.4 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E85.4 mean?
ICD-10-CM code E85.4 represents "Organ-limited amyloidosis". 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 E85.4 a billable code?
Yes, E85.4 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E85.4 in?
E85.4 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E85.4?
E85.4 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 E85.4 map to?
E85.4 maps to 60 SNOMED CT concepts: 42295001, 4645000, 16573007, 69078007, 735569003, and 55 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E85.4?
E85.4 is linked to 3 UMLS Concept Unique Identifiers: C0268392, C0494354, C4509596. 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.