FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term muscular dystrophy ID (Ontology) DOID:9884 (Human Disease)
Definition A myopathy is characterized by progressive skeletal muscle weakness degeneration.
Comment
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DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS      63
Human Disease Models (FBhh)  DOID       6
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes Human Disease Models
 muscular dystrophy      65     31      6
 ameliorates | muscular dystrophy      10       --       --
 exacerbates | muscular dystrophy      29       --       --
 model of | muscular dystrophy      28       --       --
Spanning Tree (Parents/Children)
Only view relationship:
  muscle tissue disease
   |__myopathy
       |__muscular dystrophy  387 rec.
           |__Becker muscular dystrophy 2 rec.
           |__congenital muscular dystrophy 66 rec.
           |   |__Bethlem myopathy
           |   |__congenital merosin-deficient muscular dystrophy 1A 1 rec.
           |   |__congenital muscular dystrophy 1B
           |   |__congenital muscular dystrophy due to integrin alpha-7 deficiency 1 rec.
           |   |__congenital muscular dystrophy due to LMNA mutation 24 rec.
           |   |__congenital muscular dystrophy with cataracts and intellectual disability 2 rec.
           |   |__megaconial type congenital muscular dystrophy 1 rec.
           |   |__muscular dystrophy-dystroglycanopathy(+) 30 rec.
           |   |__rigid spine muscular dystrophy 1
           |   |__Ullrich congenital muscular dystrophy(+)
           |   |__Walker-Warburg syndrome 12 rec.
           |__distal myopathy 24 rec.
           |   |__distal myopathy 1 2 rec.
           |   |__distal myopathy 3 4 rec.
           |   |__distal myopathy 4 5 rec.
           |   |__distal myopathy Tateyama type
           |   |__distal myopathy with anterior tibial onset 1 rec.
           |   |__distal myopathy with rimmed vacuoles 1 rec.
           |   |__infantile-onset distal myopathy
           |   |__Miyoshi muscular dystrophy(+) 3 rec.
           |   |__tibial muscular dystrophy 3 rec.
           |__Duchenne muscular dystrophy 16 rec.
           |__Emery-Dreifuss muscular dystrophy 25 rec.
           |   |__autosomal dominant Emery-Dreifuss muscular dystrophy 2 7 rec.
           |   |__autosomal dominant Emery-Dreifuss muscular dystrophy 4 1 rec.
           |   |__autosomal dominant Emery-Dreifuss muscular dystrophy 5 1 rec.
           |   |__autosomal dominant Emery-Dreifuss muscular dystrophy 7 1 rec.
           |   |__autosomal recessive Emery-Dreifuss muscular dystrophy 3 4 rec.
           |   |__X-linked Emery-Dreifuss muscular dystrophy 1
           |   |__X-linked Emery-Dreifuss muscular dystrophy 6 4 rec.
           |__facioscapulohumeral muscular dystrophy 6 rec.
           |   |__facioscapulohumeral muscular dystrophy 1 2 rec.
           |   |__facioscapulohumeral muscular dystrophy 2
           |   |__facioscapulohumeral muscular dystrophy 3
           |   |__facioscapulohumeral muscular dystrophy 4
           |__limb-girdle muscular dystrophy 70 rec.
           |   |__autosomal dominant limb-girdle muscular dystrophy(+) 15 rec.
           |   |__autosomal recessive limb-girdle muscular dystrophy(+) 55 rec.
           |__myotonic disease 66 rec.
           |   |__myotonic dystrophy type 1 42 rec.
           |   |__myotonic dystrophy type 2 25 rec.
           |__oculopharyngeal muscular dystrophy 46 rec.
           |__scapuloperoneal myopathy 4 rec.
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GARD:7922
ICD10CM:G71.0
MESH:D009136
MIM:158800
MIM:159050
MIM:309930
MIM:309950
MIM:310000
MIM:310095
MIM:600416
NCI:C84910
SNOMEDCT_US_2023_03_01:155095006
UMLS_CUI:C0026850