muscular dystrophy-dystroglycanopathy type B6
human disease
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muscular dystrophy-dystroglycanopathy type B6
Summary
muscular dystrophy-dystroglycanopathy type B6 is a rare disease[1].
Key Facts
- muscular dystrophy-dystroglycanopathy type B6's instance of is recorded as rare disease[2].
- muscular dystrophy-dystroglycanopathy type B6's instance of is recorded as class of disease[3].
- muscular dystrophy-dystroglycanopathy type B6 is a type of congenital muscular dystrophy[4].
- muscular dystrophy-dystroglycanopathy type B6 is a type of muscular dystrophy-dystroglycanopathy[5].
- muscular dystrophy-dystroglycanopathy type B6 is a type of genetic disease[6].
- muscular dystrophy-dystroglycanopathy type B6 is a type of autosomal recessive disease[7].
- muscular dystrophy-dystroglycanopathy type B6's health specialty is recorded as neurology[8].
- muscular dystrophy-dystroglycanopathy type B6's genetic association is recorded as LARGE1[9].
- muscular dystrophy-dystroglycanopathy type B6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110637[10].
- muscular dystrophy-dystroglycanopathy type B6's exact match is recorded as http://identifiers.org/doid/DOID:0110637[11].
- muscular dystrophy-dystroglycanopathy type B6's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].