Becker Muscular Dystrophy
Disease ID: disease_node_18873
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| Dbxref | GARD:5900, MIM:300376, ORDO:98895, SNOMEDCT_US_2023_03_01:111501005, UMLS_CUI:C0699741 |
|---|---|
| Subclassof | DOID_9884 |
| Data Source | DOID |
| Synonyms | Benign pseudohypertrophic muscular dystrophy, benign congenital myopathy |
| Doid Label | Becker muscular dystrophy |
| Doid Description | 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. OMIM mapping confirmed by DO. [SN]. |
| Has Symptom | SYMP_0000094 |
| Disease Node Id | disease_node_18873 |
| Doid Id | DOID_9883 |
| Label | Becker Muscular Dystrophy |
- Outgoing r'ship
HAS_SYMPTOMto/from Muscle Weakness(ID:disease_node_9835;disease_node_21022) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Muscular Dystrophies(ID:disease_node_5318) (Disease)