FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term muscle tissue disease ID (Ontology) DOID:66 (Human Disease)
Definition A muscular disease located in the muscle tissue.
Comment
Links to External Ontologies
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)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 for disease ribbon | tooth and nail syndrome       2
 for disease ribbon | X-linked Aarskog syndrome       1
 model of | tooth and nail syndrome       2
 model of | X-linked Aarskog syndrome       1
Spanning Tree (Parents/Children)
Only view relationship:
  musculoskeletal system disease
   |__muscular disease
       |__muscle tissue disease  690 rec.
           |__distal arthrogryposis 46 rec.
           |   |__congenital contractural arachnodactyly 2 rec.
           |   |__distal arthrogryposis type 1(+) 12 rec.
           |   |__distal arthrogryposis type 2B(+) 7 rec.
           |   |__distal arthrogryposis type 3 1 rec.
           |   |__distal arthrogryposis type 4
           |   |__distal arthrogryposis type 5 1 rec.
           |   |__distal arthrogryposis type 5D 15 rec.
           |   |__distal arthrogryposis type 6
           |   |__distal arthrogryposis type 7 1 rec.
           |   |__distal arthrogryposis type 10
           |   |__Freeman-Sheldon syndrome(+) 9 rec.
           |__malignant hyperthermia
           |__myopathy 648 rec.
           |   |__congenital myopathy(+) 100 rec.
           |   |__GNE myopathy
           |   |__King Denborough syndrome 1 rec.
           |   |__mitochondrial myopathy(+) 44 rec.
           |   |__muscular atrophy
           |   |__muscular dystrophy(+) 387 rec.
           |   |__myofascial pain syndrome
           |   |__myofibrillar myopathy(+) 45 rec.
           |   |__myoglobinuria 1 rec.
           |   |__myopathy of extraocular muscle
           |   |__myopathy with extrapyramidal signs 6 rec.
           |   |__myositis(+) 6 rec.
           |   |__neurogenic scapuloperoneal syndrome Kaeser type
           |   |__oculopharyngodistal myopathy(+) 2 rec.
           |   |__reducing body myopathy 1A 7 rec.
           |   |__reducing body myopathy 1B 6 rec.
           |   |__rhabdomyolysis-myalgia syndrome
           |   |__tubular aggregate myopathy 1 1 rec.
           |   |__tubular aggregate myopathy 2 1 rec.
           |   |__X-linked myopathy with excessive autophagy 1 rec.
           |__myostatin-related muscle hypertrophy 1 rec.
           |__myotonia congenita 16 rec.
           |   |__Becker disease 1 rec.
           |   |__Thomsen disease 1 rec.
           |__rippling muscle disease 1
           |__rippling muscle disease 2
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a muscular disease
Part of
hide Synonyms & Secondary IDs
Synonyms
Secondary IDs
hide External Crossreferences & Linkouts