WormBase Tree Display for DO_term: DOID:0111223
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DOID:0111223 | Name | centronuclear myopathy 1 | |||
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Status | Valid | ||||
Definition | An autosomal dominant centronuclear myopathy characterized by slowly progressive muscle wasting and weakness involving mainly the limb girdle, trunk, and neck muscles that has_material_basis_in heterozygous mutation in DNM2 on 19p13.2. | ||||
Synonym | Exact | CNM1 | |||
Parent | Is_a | DOID:0111217 | |||
DB_info | Database | OMIM | disease | 160150 | |
Attribute_of | Gene_by_orthology | WBGene00001130 |