WormBase Tree Display for DO_term: DOID:0081338
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DOID:0081338 | Name | myofibrillar myopathy 11 | |||
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Status | Valid | ||||
Definition | A 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. | ||||
Parent | Is_a | DOID:0080307 | |||
DB_info | Database | OMIM | disease | 619178 | |
Attribute_of | Gene_by_orthology | WBGene00006781 |