E85.1
BillableNeuropathic heredofamilial amyloidosis
Neuropathic heredofamilial amyloidosis
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Amyloid polyneuropathy (Portuguese)
- Transthyretin-related (ATTR) familial amyloid polyneuropathy
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Also Known As / Clinical Terms
SNOMED CT
- Amyloidosis, Indiana-Maryland type4463009
- Familial amyloid polyneuropathy type II4463009
- Familial amyloid polyneuropathy, 84 Ser-for-Ile4463009
- Familial amyloid polyneuropathy, Indiana-Swiss type4463009
- Familial amyloid polyneuropathy, type II4463009
- German type amyloid polyneuropathy4463009
- Hereditary neuropathic amyloidosis, type II4463009
- Indiana-Maryland type amyloid polyneuropathy4463009
- Rakavina type amyloidosis4463009
- Swiss type amyloid polyneuropathy4463009
- Familial amyloid polyneuropathy, 60 Ala-for-Thr5134006
- Familial amyloid polyneuropathy, Appalachian type5134006
- Familial amyloid polyneuropathy, type VI5134006
- Familial amyloid polyneuropathy type III9133005
- Familial amyloid polyneuropathy, Iowa type9133005
- Iowa type amyloid polyneuropathy9133005
- Iowa type amyloidosis9133005
- Van Allen type amyloid polyneuropathy9133005
- van Allen type amyloidosis9133005
- Familial amyloid polyneuropathy, 33 Ile-for-Phe41590007
- Familial amyloid polyneuropathy, Jewish type41590007
- Jewish type amyloid polyneuropathy41590007
- AF type amyloidosis42295001
- Familial amyloid polyneuropathy42295001
- Familial neuropathic amyloidosis42295001
- Familial polyneuropathic amyloidosis42295001
- Neuropathic heredofamilial amyloidosis42295001
- Amyloidosis VI45639009
- Hereditary cerebral amyloid angiopathy, Icelandic type45639009
- Hereditary cerebral haemorrhage with amyloidosis - Icelandic type45639009
- Hereditary cerebral hemorrhage with amyloidosis - Icelandic type45639009
- Hereditary cystatin C amyloid angiopathy45639009
- Iceland type amyloidosis45639009
- Icelandic type amyloidosis45639009
- Amyloid polyneuropathy193187004
- Polyneuropathy due to amyloidosis193187004
- Polyneuropathy in amyloidosis193187004
- Neuropathy associated with dysproteinaemias230585004
- Neuropathy associated with dysproteinemias230585004
- CAA - Cerebral amyloid angiopathy230724001
- Cerebral amyloid angiopathy230724001
- Congophilic angiopathy230724001
- Hereditary cerebrovascular amyloidosis237867001
- Localised hereditary amyloidosis237869003
- Localized hereditary amyloidosis237869003
- Organ limited hereditary amyloidosis237869003
- Amyloid polyneuropathy type I398229007
- Amyloidosis, type I398229007
- Andrade syndrome398229007
- Andrade type amyloid polyneuropathy398229007
- Corino de Andrade paramyloidosis398229007
- Familial amyloid neuropathy, Andrade type398229007
- Familial amyloid neuropathy, Portuguese type398229007
- Familial amyloid polyneuropathy, 30 Met-for-Val398229007
- Hereditary amyloid polyneuropathy Portuguese type398229007
- Hereditary neuropathic amyloidosis, type I398229007
- Japanese type amyloid polyneuropathy398229007
- Portuguese polyneuritic amyloidosis398229007
- Portuguese type amyloid polyneuropathy398229007
- Swedish type amyloid polyneuropathy398229007
- Wohlwill-Corino Andrade syndrome398229007
- Heredofamilial systemic amyloidosis affecting skin402459005
- Familial amyloid polyneuropathy affecting skin402460000
- Familial amyloid polyneuropathy with cutaneous amyloidosis402460000
- Systemic amyloidosis affecting skin402719006
- HCHWA - hereditary cerebral haemorrhage with amyloidosis724357007
- HCHWA - hereditary cerebral hemorrhage with amyloidosis724357007
- Hereditary cerebral haemorrhage with amyloidosis724357007
- Hereditary cerebral hemorrhage with amyloidosis724357007
- Disorder of glomerulus due to familial disease1148882003
- Glomerular disease due to familial disease1148882003
- Disorder of glomerulus due to familial amyloid polyneuropathy1187554000
- Disorder of glomerulus due to neuropathic heredofamilial amyloidosis1187554000
- Glomerular disorder due to neuropathic heredofamilial amyloidosis1187554000
- Disorder of glomerulus due to amyloidosis1187557007
- Glomerular disorder due to amyloidosis1187557007
- ATTRv amyloidosis1354544003
- Familial TTR-related amyloidosis1354544003
- Familial transthyretin-related amyloidosis1354544003
- Hereditary ATTR amyloidosis1354544003
- Hereditary TTR amyloid polyneuropathy1354544003
- Hereditary TTR amyloidosis1354544003
- Hereditary transthyretin amyloid polyneuropathy1354544003
- Hereditary transthyretin related amyloidosis1354544003
- hATTR - hereditary transthyretin related amyloidosis1354544003
UMLS
- AF type amyloidosisC0206245
- Amyloid Neuropathies, FamilialC0206245
- Amyloid Neuropathy, FamilialC0206245
- Amyloid Polyneuropathies, FamilialC0206245
- Amyloid Polyneuropathy, FamilialC0206245
- Amyloidoses, Hereditary NeuropathicC0206245
- Amyloidosis, Hereditary NeuropathicC0206245
- Familial Amyloid NeuropathiesC0206245
- Familial Amyloid NeuropathyC0206245
- Familial Amyloid PolyneuropathiesC0206245
- Familial Amyloid PolyneuropathyC0206245
- Familial amyloid polyneuropathyC0206245
- Familial amyloid polyneuropathy (disorder)C0206245
- Familial neuropathic amyloidosisC0206245
- Familial polyneuropathic amyloidosisC0206245
- Hereditary Neuropathic AmyloidosesC0206245
- Hereditary Neuropathic AmyloidosisC0206245
- Hereditary neuropathic amyloidosisC0206245
- Neuropathic Amyloidoses, HereditaryC0206245
- Neuropathic Amyloidosis, HereditaryC0206245
- Neuropathic heredofamilial amyloidosisC0206245
- Neuropathies, Familial AmyloidC0206245
- Neuropathy, Familial AmyloidC0206245
- Polyneuropathies, Familial AmyloidC0206245
- Polyneuropathy, Familial AmyloidC0206245
- amyloid familial polyneuropathiesC0206245
- familial amyloid polyneuropathyC0206245
- Amyloid polyneuropathy (Portuguese)C2874309
- Transthyretin-related (ATTR) familial amyloid polyneuropathyC4509022
Frequently Asked Questions
What is ICD-10 code E85.1?
ICD-10-CM code E85.1 represents "Neuropathic heredofamilial amyloidosis". It is a billable/specific code that can be used on a claim.
Is E85.1 a billable code?
Yes, E85.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E85.1 in?
E85.1 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E85.1?
E85.1 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 E85.1 map to?
E85.1 maps to 20 SNOMED CT concepts: 42295001, 1354544003, 193187004, 398229007, 45639009, and 15 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E85.1?
E85.1 is linked to 3 UMLS Concept Unique Identifiers: C0206245, C2874309, C4509022. 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.