Ullrich congenital muscular dystrophy
Ullrich congenital muscular dystrophy (UCMD) is characterized by early-onset, generalized and slowly progressive muscle weakness, multiple proximal joint contractures, marked hypermobility of the distal joints and normal intelligence
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Ullrich congenital muscular dystrophy
Summary
Ullrich congenital muscular dystrophy is a designated intractable/rare disease[1]. It draws 58 Wikipedia views per month (designated_intractable_rare_disease category, ranking #158 of 201).[2]
Key Facts
- Ullrich congenital muscular dystrophy's instance of is recorded as designated intractable/rare disease[3].
- Ullrich congenital muscular dystrophy's instance of is recorded as rare disease[4].
- Ullrich congenital muscular dystrophy's instance of is recorded as class of disease[5].
- Otto Ullrich is named after Ullrich congenital muscular dystrophy[6].
- Ullrich congenital muscular dystrophy is a type of congenital muscular dystrophy[7].
- Ullrich congenital muscular dystrophy is a type of genetic disease[8].
- Ullrich congenital muscular dystrophy is a type of autosomal dominant disease[9].
- Ullrich congenital muscular dystrophy is a type of autosomal recessive disease[10].
- Ullrich congenital muscular dystrophy is a type of Collagen VI myopathy[11].
- Ullrich congenital muscular dystrophy's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/3999[12].
- Ullrich congenital muscular dystrophy's NCI Thesaurus ID is recorded as C123438[13].
- Ullrich congenital muscular dystrophy's genetic association is recorded as COL6A2[14].
- Ullrich congenital muscular dystrophy's genetic association is recorded as COL6A1[15].
- Ullrich congenital muscular dystrophy's genetic association is recorded as COL6A3[16].
- Ullrich congenital muscular dystrophy's genetic association is recorded as COL12A1[17].
- Ullrich congenital muscular dystrophy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050558[18].
- Ullrich congenital muscular dystrophy's exact match is recorded as http://identifiers.org/doid/DOID:0050558[19].
- Ullrich congenital muscular dystrophy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_75840[20].
- Ullrich congenital muscular dystrophy's on focus list of Wikimedia project is recorded as WikiProject Medicine[21].
Why It Matters
Ullrich congenital muscular dystrophy draws 58 Wikipedia views per month (designated_intractable_rare_disease category, ranking #158 of 201).[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[22] It is known by 13 alternative names across languages and contexts.[23]