FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term distal arthrogryposis ID (Ontology) DOID:0050646 (Human Disease)
Definition A muscle tissue disease characterized by congenital joint contractures of hand and feet.
Also Known As "Arthrogryposis Multiplex Congenita"
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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       5
Human Disease Models (FBhh)  DOID       1
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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Relevant FlyBase reports
 Alleles Genes Human Disease Models
 distal arthrogryposis       5      2      1
 model of | distal arthrogryposis       5       --       --
Spanning Tree (Parents/Children)
Only view relationship: 
  muscular disease
   |__muscle tissue disease
       |__distal arthrogryposis  46 rec.
           |__congenital contractural arachnodactyly 2 rec.
           |__distal arthrogryposis type 1 12 rec.
           |   |__distal arthrogryposis type 1A 4 rec.
           |   |__distal arthrogryposis type 1B
           |   |__distal arthrogryposis type 1C 3 rec.
           |__distal arthrogryposis type 2B 7 rec.
           |   |__distal arthrogryposis type 2B1 1 rec.
           |   |__distal arthrogryposis type 2B2 1 rec.
           |   |__distal arthrogryposis type 2B3 3 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.
               |__autosomal recessive Whistling face syndrome
               |__distal arthrogryposis type 2A 9 rec.
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Is a muscle tissue disease
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Synonyms
  • "Arthrogryposis Multiplex Congenita" EXACT
Secondary IDs
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GARD:786
MIM:PS108120
ORDO:1147
ORDO:97120