multiminicore myopathy
Multi-minicore Disease (MmD) is a hereditary neuromuscular disorder characterized by multiple cores on muscle biopsy and clinical features of a congenital myopathy
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multiminicore myopathy
Summary
multiminicore myopathy is a rare disease[1]. It draws 2 Wikipedia views per month (rare_disease category, ranking #237 of 627).[2]
Key Facts
- multiminicore myopathy's instance of is recorded as rare disease[3].
- multiminicore myopathy's instance of is recorded as class of disease[4].
- multiminicore myopathy's subclass of is recorded as congenital myopathy[5].
- multiminicore myopathy's Commons category is recorded as Multicore myopathy[6].
- multiminicore myopathy's KEGG ID is recorded as H01310[7].
- multiminicore myopathy's Orphanet ID is recorded as 598[8].
- multiminicore myopathy's genetic association is recorded as RYR1[9].
- multiminicore myopathy's genetic association is recorded as SELENON[10].
- multiminicore myopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_598[11].
- multiminicore myopathy's UMLS CUI is recorded as C0270962[12].
- multiminicore myopathy's ICD-10-CM is recorded as G71.2[13].
- multiminicore myopathy's GARD rare disease ID is recorded as 9130[14].
- multiminicore myopathy's Mondo ID is recorded as MONDO_0018948[15].
Why It Matters
multiminicore myopathy draws 2 Wikipedia views per month (rare_disease category, ranking #237 of 627).[2]