FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term muscular dystrophy-dystroglycanopathy ID (Ontology) DOID:0112374 (Human Disease)
Definition A congenital muscular dystrophy characterized by muscular dystrophy resulting from defective glycosylation of dystroglycan.
Also Known As "MDDG"
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)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       9
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
 muscular dystrophy-dystroglycanopathy       9      4
 exacerbates | muscular dystrophy-dystroglycanopathy       4       --
 model of | muscular dystrophy-dystroglycanopathy       6       --
Spanning Tree (Parents/Children)
Only view relationship: 
physical disorder___
muscular dystrophy__|
                    congenital muscular dystrophy
                     |__muscular dystrophy-dystroglycanopathy  30 rec.
                         |__congenital muscular dystrophy-dystroglycanopathy type A 16 rec.
                         |   |__congenital muscular dystrophy-dystroglycanopathy type A1 5 rec.
                         |   |__congenital muscular dystrophy-dystroglycanopathy type A2 2 rec.
                         |   |__congenital muscular dystrophy-dystroglycanopathy type A3 1 rec.
                         |   |__congenital muscular dystrophy-dystroglycanopathy type A5 1 rec.
                         |   |__congenital muscular dystrophy-dystroglycanopathy type A6 3 rec.
                         |   |__congenital muscular dystrophy-dystroglycanopathy type A7
                         |   |__congenital muscular dystrophy-dystroglycanopathy type A8
                         |   |__congenital muscular dystrophy-dystroglycanopathy type A9 2 rec.
                         |   |__congenital muscular dystrophy-dystroglycanopathy type A10
                         |   |__congenital muscular dystrophy-dystroglycanopathy type A11 1 rec.
                         |   |__congenital muscular dystrophy-dystroglycanopathy type A12
                         |   |__congenital muscular dystrophy-dystroglycanopathy type A13 4 rec.
                         |   |__congenital muscular dystrophy-dystroglycanopathy type A14 1 rec.
                         |   |__Fukuyama congenital muscular dystrophy
                         |__muscular dystrophy-dystroglycanopathy type B 12 rec.
                         |   |__muscular dystrophy-dystroglycanopathy type B1 3 rec.
                         |   |__muscular dystrophy-dystroglycanopathy type B2 2 rec.
                         |   |__muscular dystrophy-dystroglycanopathy type B3 1 rec.
                         |   |__muscular dystrophy-dystroglycanopathy type B4
                         |   |__muscular dystrophy-dystroglycanopathy type B5 1 rec.
                         |   |__muscular dystrophy-dystroglycanopathy type B6 3 rec.
                         |   |__muscular dystrophy-dystroglycanopathy type B14 1 rec.
                         |   |__muscular dystrophy-dystroglycanopathy type B15 1 rec.
                         |__muscular dystrophy-dystroglycanopathy type C8
                         |__muscular dystrophy-dystroglycanopathy type C12
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Is a congenital muscular dystrophy
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Synonyms
  • "MDDG" EXACT OMO:0003012
Secondary IDs
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ICD10CM:G71.2
ORDO:370953