centronuclear myopathy
myopathy characterized by abnormally located nuclei in skeletal muscle cells
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centronuclear myopathy
Summary
centronuclear myopathy is a rare disease[1]. It draws 138 Wikipedia views per month (rare_disease category, ranking #133 of 627).[2]
Key Facts
- centronuclear myopathy's instance of is recorded as rare disease[3].
- centronuclear myopathy's instance of is recorded as class of disease[4].
- centronuclear myopathy's subclass of is recorded as muscular disease[5].
- centronuclear myopathy's subclass of is recorded as congenital myopathy[6].
- centronuclear myopathy's Commons category is recorded as Centronuclear myopathy[7].
- centronuclear myopathy's OMIM ID is recorded as 160150[8].
- centronuclear myopathy's OMIM ID is recorded as 310400[9].
- centronuclear myopathy's OMIM ID is recorded as 255200[10].
- centronuclear myopathy's OMIM ID is recorded as 614807[11].
- centronuclear myopathy's OMIM ID is recorded as 615959[12].
- centronuclear myopathy's DiseasesDB is recorded as 31983[13].
- centronuclear myopathy's Freebase ID is recorded as /m/0cx6xn[14].
- centronuclear myopathy's KEGG ID is recorded as H00700[15].
- centronuclear myopathy's GeneReviews ID is recorded as NBK1432[16].
- centronuclear myopathy's eMedicine ID is recorded as 1175852[17].
- centronuclear myopathy's Disease Ontology ID is recorded as DOID:14717[18].
- centronuclear myopathy's Orphanet ID is recorded as 596[19].
- centronuclear myopathy's Orphanet ID is recorded as 69189[20].
- centronuclear myopathy's Orphanet ID is recorded as 69186[21].
- centronuclear myopathy's Orphanet ID is recorded as 595[22].
- centronuclear myopathy's NCI Thesaurus ID is recorded as C84648[23].
- centronuclear myopathy's health specialty is recorded as neurology[24].
- centronuclear myopathy's genetic association is recorded as SPEG[25].
- centronuclear myopathy's genetic association is recorded as MYF6[26].
- centronuclear myopathy's genetic association is recorded as MTM1[27].
Why It Matters
centronuclear myopathy draws 138 Wikipedia views per month (rare_disease category, ranking #133 of 627).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] It is known by 6 alternative names across languages and contexts.[29]