FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term congenital structural myopathy ID (Ontology) DOID:422 (Human Disease)
Definition A myopathy that is characterized by hypotonia, muscle weakness, and delayed development of motor skills.
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DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       4
Human Disease Models (FBhh)  DOID       1
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Relevant FlyBase reports
 Alleles Genes Human Disease Models
 congenital structural myopathy       5      1      1
 model of | congenital structural myopathy       5       --       --
Spanning Tree (Parents/Children)
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disease
myopathy
 |__congenital myopathy__
 |__physical disorder____|
                         congenital structural myopathy  25 rec.
                          |__centronuclear myopathy 18 rec.
                              |__autosomal dominant centronuclear myopathy(+) 3 rec.
                              |__autosomal recessive centronuclear myopathy(+) 7 rec.
                              |__centronuclear myopathy X-linked 3 rec.
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Is a physical disorder
congenital myopathy
Part of
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Synonyms
Secondary IDs
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MESH:D020914
NCI:C84648
UMLS_CUI:C0752282