Familial amyloid cardiomyopathy
Transthyretin (TTR)-related familial amyloidotic cardiomyopathy is a hereditary TTR-related systemic amyloidosis (ATTR) with predominant cardiac involvement resulting from myocardial infiltration of abnormal amyloid protein
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Familial amyloid cardiomyopathy
Summary
Familial amyloid cardiomyopathy is a class of disease[1]. It draws 51 Wikipedia views per month (class_of_disease category, ranking #597 of 1,968).[2]
Key Facts
- Familial amyloid cardiomyopathy's instance of is recorded as class of disease[3].
- Familial amyloid cardiomyopathy's subclass of is recorded as Amyloid cardiomyopathy[4].
- Familial amyloid cardiomyopathy's subclass of is recorded as familial cardiomyopathy[5].
- Familial amyloid cardiomyopathy's Freebase ID is recorded as /m/0hrd2r8[6].
- Familial amyloid cardiomyopathy's Orphanet ID is recorded as 85451[7].
- Familial amyloid cardiomyopathy's NCI Thesaurus ID is recorded as C165489[8].
- Familial amyloid cardiomyopathy's genetic association is recorded as TTR[9].
- Familial amyloid cardiomyopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_85451[10].
- Familial amyloid cardiomyopathy's UMLS CUI is recorded as C4275067[11].
- Familial amyloid cardiomyopathy's ICD-10-CM is recorded as I43.1*[12].
- Familial amyloid cardiomyopathy's ICD-10-CM is recorded as E85.4+[13].
- Familial amyloid cardiomyopathy's Mondo ID is recorded as MONDO_0019441[14].
- Familial amyloid cardiomyopathy's Microsoft Academic ID is recorded as 2778295755[15].
Why It Matters
Familial amyloid cardiomyopathy draws 51 Wikipedia views per month (class_of_disease category, ranking #597 of 1,968).[2]