nemaline myopathy
congenital structural myopathy characterized by generally non-progressive muscle weakness of varying severity
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nemaline myopathy
Summary
nemaline myopathy is a rare disease[1]. It draws 250 Wikipedia views per month (rare_disease category, ranking #208 of 627).[2]
Key Facts
- nemaline myopathy's instance of is recorded as rare disease[3].
- nemaline myopathy's instance of is recorded as class of disease[4].
- nemaline myopathy is a type of congenital structural myopathy[5].
- nemaline myopathy is a type of non-dystrophic myopathy[6].
- nemaline myopathy is a type of disease[7].
- nemaline myopathy's Commons category is recorded as Nemaline myopathy[8].
- nemaline myopathy's health specialty is recorded as neurology[9].
- nemaline myopathy's genetic association is recorded as ACTA1[10].
- nemaline myopathy's genetic association is recorded as LMOD3[11].
- nemaline myopathy's genetic association is recorded as NEB[12].
- nemaline myopathy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_3191[13].
- nemaline myopathy's exact match is recorded as http://identifiers.org/doid/DOID:3191[14].
- nemaline myopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_607[15].
- nemaline myopathy's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
nemaline myopathy draws 250 Wikipedia views per month (rare_disease category, ranking #208 of 627).[2] It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[17] It is known by 14 alternative names across languages and contexts.[18]