early-onset myopathy with fatal cardiomyopathy
human disease
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early-onset myopathy with fatal cardiomyopathy
Summary
early-onset myopathy with fatal cardiomyopathy is a rare disease[1].
Key Facts
- early-onset myopathy with fatal cardiomyopathy's instance of is recorded as rare disease[2].
- early-onset myopathy with fatal cardiomyopathy's instance of is recorded as class of disease[3].
- early-onset myopathy with fatal cardiomyopathy's subclass of is recorded as non-dystrophic myopathy[4].
- early-onset myopathy with fatal cardiomyopathy's subclass of is recorded as qualitative or quantitative defects of titin[5].
- early-onset myopathy with fatal cardiomyopathy's subclass of is recorded as neuromuscular disease with dilated cardiomyopathy[6].
- early-onset myopathy with fatal cardiomyopathy's MeSH descriptor ID is recorded as C567129[7].
- early-onset myopathy with fatal cardiomyopathy's OMIM ID is recorded as 611705[8].
- early-onset myopathy with fatal cardiomyopathy's Orphanet ID is recorded as 289377[9].
- early-onset myopathy with fatal cardiomyopathy's genetic association is recorded as TTN[10].
- early-onset myopathy with fatal cardiomyopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_289377[11].
- early-onset myopathy with fatal cardiomyopathy's UMLS CUI is recorded as C2673677[12].
- early-onset myopathy with fatal cardiomyopathy's ICD-10-CM is recorded as G71.8[13].
- early-onset myopathy with fatal cardiomyopathy's Mondo ID is recorded as MONDO_0012714[14].
- early-onset myopathy with fatal cardiomyopathy's Genetics Home Reference Conditions ID is recorded as early-onset-myopathy-with-fatal-cardiomyopathy[15].