Bethlem myopathy
human disease
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Bethlem myopathy
Summary
Bethlem myopathy is a designated intractable/rare disease[1]. It draws 47 Wikipedia views per month (designated_intractable_rare_disease category, ranking #135 of 201).[2]
Key Facts
- Bethlem myopathy's instance of is recorded as designated intractable/rare disease[3].
- Bethlem myopathy's instance of is recorded as class of disease[4].
- Jaap Bethlem is named after Bethlem myopathy[5].
- Bethlem myopathy is a type of congenital muscular dystrophy[6].
- Bethlem myopathy is a type of Collagen VI myopathy[7].
- Bethlem myopathy's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4005[8].
- Bethlem myopathy's NCI Thesaurus ID is recorded as C126688[9].
- Bethlem myopathy's genetic association is recorded as COL6A2[10].
- Bethlem myopathy's genetic association is recorded as COL6A1[11].
- Bethlem myopathy's genetic association is recorded as COL6A3[12].
- Bethlem myopathy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050663[13].
- Bethlem myopathy's exact match is recorded as http://identifiers.org/doid/DOID:0050663[14].
- Bethlem myopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_610[15].
- Bethlem myopathy's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
Bethlem myopathy draws 47 Wikipedia views per month (designated_intractable_rare_disease category, ranking #135 of 201).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[17] It is known by 13 alternative names across languages and contexts.[18]