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Ullrich congenital muscular dystrophy
Classification and external resources
OMIM	254090
DiseasesDB	33679

Ullrich congenital muscular dystrophy is a form of congenital muscular dystrophy.

It is associated with variants of type VI collagen.^[1]

[edit] References

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AD	Limb-girdle muscular dystrophy 1 · Oculopharyngeal · Facioscapulohumeral · Myotonic · Distal (most)

AR	Limb-girdle muscular dystrophy 2 · Congenital (Fukuyama, Ullrich)

XR	dystrophin (Becker's, Duchenne) · Emerin Emery-Dreifuss

Other structural

collagen disease (Bethlem myopathy) · PTP disease (X-linked MTM) · adaptor protein disease (BIN1-linked centronuclear myopathy) · cytoskeleton disease (Nemaline myopathy, Zaspopathy)

Myotonia	Myotonia congenita · Thomsen disease · Neuromyotonia/Isaacs syndrome · Paramyotonia congenita

Periodic paralysis	Hypokalemic · Hyperkalemic

Other	Central core disease

Other

muscle, DF+DRCT navs: anat/hist/physio, acquired myopathy/congenital myopathy/neoplasia, symptoms+signs/eponymous, proc

Genetic disorder: Scleroprotein disease

Genetic	COL1: Osteogenesis imperfecta · Ehlers-Danlos syndrome, types 1,2,&7 COL2: Hypochondrogenesis · Achondrogenesis type 2 · Stickler syndrome · Marshall syndrome · Spondyloepiphyseal dysplasia congenita (see also C2/11) COL3: Ehlers-Danlos syndrome, types 3&4 (Sack-Barabas syndrome) COL4: Alport syndrome COL5: Ehlers-Danlos syndrome, types 1&2 COL6: Bethlem myopathy · Ullrich congenital muscular dystrophy COL7: Epidermolysis bullosa dystrophica COL8: Fuchs' dystrophy COL9: Multiple epiphyseal dysplasia COL10: Schmid metaphyseal chondrodysplasia COL11: Weissenbacher-Zweymüller syndrome · Otospondylomegaepiphyseal dysplasia (see also C2/11) COL17: Bullous pemphigoid

Autoimmune	Goodpasture's syndrome

see also proteins