wild-type transthyretin amyloid
human disease
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Summary
wild-type transthyretin amyloid is a class of disease[1]. It draws 791 Wikipedia views per month (class of disease category, ranking #606 of 1,968).[2]
Key Facts
- Subclass of: amyloidosis[3], non-familial restrictive cardiomyopathy[4]
- Prevalence: 0.0003[5]
- ICD-9-CM: 277.39[6]
- Age of onset: adult onset[7], late onset[8]
- Exact match: http://www.orpha.net/ORDO/Orphanet_330001[9]
- Has phenotype: hypertrophic cardiomyopathy[10], myocardial infarction[11], pleural effusion[12], EKG abnormal[13], interstitial lung disease[14], Q141816436[15], pulmonary edema[16], sensory peripheral neuropathy[17], chronic diarrhea[18], hepatomegaly[19], Q141815158[20], Q141815185[21], fecal incontinence[22], elevated alkaline phosphatase[23]
- P14914: D330001[24]
Why It Matters
wild-type transthyretin amyloid is known by 14 alternative names across languages and contexts.[25]