E85.2 HEREDOFAMILIAL AMYLOIDOSIS, UNSPECIFIED

Synonyms

• ABri amyloidosis
• ADan amyloidosis
• AGel amyloidosis
• Amyloid myopathy
• Amyloid nephropathy
• Amyloid nephropathy
• Autosomal dominant beta2-microglobulinic amyloidosis
• Cerebral amyloid angiopathy
• Cerebral amyloid angiopathy
• Cerebral amyloid angiopathy
• Cerebral amyloid angiopathy
• Cryopyrin associated periodic syndrome
• Familial amyloid nephropathy with urticaria AND deafness
• Familial lichen amyloidosis
• Familial localized cutaneous amyloidosis
• Familial non-neuropathic amyloidosis
• Familial visceral amyloidosis, Ostertag type
• Hereditary amyloidosis
• Hereditary cerebrovascular amyloidosis
• Hereditary systemic amyloidosis
• Heredofamilial systemic amyloidosis affecting skin
• ITM2B-related amyloidosis
• Localized hereditary amyloidosis
• Localized hereditary amyloidosis
• Localized hereditary cardiac amyloidosis
• Primary familial amyloid myopathy
• Primary localized cutaneous amyloidosis
• Prion protein systemic amyloidosis
• Systemic amyloidosis affecting skin
• Systemic amyloidosis affecting skin

Diagnostic Related Group(s)

The code E85.2 is grouped in the following Diagnostic Related Group(s) MS-DRG V42.0

1. Connective Tissue Disorders With Mcc (545)
2. Connective Tissue Disorders With Cc (546)
3. Connective Tissue Disorders Without Cc/mcc (547)

Crosswalk Information

ICD-10 Code		ICD-9 Code	ICD-9 Description
E85.2		277.39	Amyloidosis NEC

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