WormBase Tree Display for DO_term: DOID:9883
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| DOID:9883 | Name | Becker muscular dystrophy | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A muscular dystrophy that involves slowly worsening muscle weakness of the legs and pelvis, and has_material_basis_in X-linked recessive inheritance of mutation in the dystrophin gene on chromosome Xp21. | ||||
| Comment | OMIM mapping confirmed by DO. | ||||
| Synonym | Exact | Benign pseudohypertrophic muscular dystrophy | |||
| benign congenital myopathy | |||||
| Parent | Is_a | DOID:9884 | |||
| DB_info | Database | OMIM | disease | 300376 | |
| Attribute_of | Gene_by_orthology | WBGene00001131 |
