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WormBase Tree Display for DO_term: DOID:11723

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Name Class

DOID:11723NameDuchenne muscular dystrophy
StatusValid
DefinitionA muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy.
CommentOMIM mapping confirmed by DO.
SynonymExactMuscular dystrophy, Duchenne
ParentIs_aDOID:9884
DOID:0080012
DB_infoDatabaseOMIMdisease310200
Disease_model_annotationWBDOannot00000094
WBDOannot00000107
WBDOannot00000110
WBDOannot00000114
WBDOannot00000220
WBDOannot00000286
WBDOannot00000287
WBDOannot00000289
WBDOannot00000290
WBDOannot00000291
WBDOannot00000292
WBDOannot00000293
WBDOannot00000294
WBDOannot00000295
WBDOannot00000320
WBDOannot00000418
WBDOannot00000419
WBDOannot00000420
WBDOannot00000421
WBDOannot00000422
WBDOannot00000423
WBDOannot00000424
WBDOannot00000425
WBDOannot00000426
WBDOannot00000427
WBDOannot00000428
WBDOannot00000429
WBDOannot00000430
WBDOannot00000431
WBDOannot00000617
WBDOannot00000745
WBDOannot00000746
WBDOannot00000747
WBDOannot00001434
WBDOannot00001438
Attribute_ofGene_by_biologyWBGene00000542
WBGene00004830
WBGene00017866
WBGene00001248
WBGene00004905
WBGene00000500
WBGene00000832
WBGene00001116
WBGene00001131
WBGene00001187
WBGene00006062
WBGene00001115
WBGene00001948
Gene_by_orthologyWBGene00000961
WBGene00001131
WBGene00002081
WBGene00012319
WBGene00016661
WBGene00018943
WBGene00019476
WBGene00019478
Disease_modifier_geneWBGene00000282
WBGene00006801
WBGene00001116
WBGene00001115
Disease_model_variationWBVar00089610
WBVar00054722
WBVar00091590
WBVar00054752
WBVar00278332
WBVar00296796
WBVar00054742
WBVar00054717
WBVar00145104
WBVar00250832
WBVar00054732
WBVar00054737
WBVar00054767
Disease_modifier_variationWBVar00143949
WBVar00089216
Disease_model_strainWBStrain00024341
WBStrain00024340
WBStrain00024343
Disease_model_genotypeWBGenotype00000013
WBGenotype00000012
Molecule_modifierWBMol:00002862
WBMol:00001788
WBMol:00004976
WBMol:00004999
WBMol:00007885
WBMol:00008020
WBMol:00008021