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WormBase Tree Display for DO_term: DOID:0081338

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Name Class

DOID:0081338Namemyofibrillar myopathy 11
StatusValid
DefinitionA myofibrillar myopathy that is characterized by onset of slowly progressive proximal muscle weakness in the first decade of life and that has_material_basis_in homozygous or compound heterozygous mutation in the UNC45B gene on chromosome 17q11.
ParentIs_aDOID:0080307
DB_infoDatabaseOMIMdisease619178
Attribute_ofGene_by_orthologyWBGene00006781