loading...| Preferred Name |
Becker muscular dystrophy |
|
| Synonyms |
benign congenital myopathy |
|
| Definitions |
OMIM mapping confirmed by DO. [SN]. 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. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_9883 |
|
| comment |
OMIM mapping confirmed by DO. [SN]. |
|
| database_cross_reference |
OMIM:300376 UMLS_CUI:C0699741 SNOMEDCT_US_2023_03_01:111501005 GARD:5900 ORDO:98895 |
|
| 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. |
|
| has exact synonym |
benign congenital myopathy Benign pseudohypertrophic muscular dystrophy |
|
| has symptom | ||
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:9883 |
|
| in_subset | ||
| label |
Becker muscular dystrophy |
|
| notation |
DOID:9883 |
|
| prefLabel |
Becker muscular dystrophy |
|
| subClassOf |