FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term autosomal dominant limb-girdle muscular dystrophy ID (Ontology) DOID:0110273 (Human Disease)
Definition A limb-girdle muscular dystrophy that has_material_basis_in autosomal dominant inheritance.
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Human Disease Models (FBhh)  DOID       1
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 Human Disease Models
 autosomal dominant limb-girdle muscular dystrophy       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease______
muscular dystrophy                  |
 |__limb-girdle muscular dystrophy__|
                                    autosomal dominant limb-girdle muscular dystrophy  15 rec.
                                     |__autosomal dominant limb-girdle muscular dystrophy type 1 3 rec.
                                     |__autosomal dominant limb-girdle muscular dystrophy type 1H
                                     |__autosomal dominant limb-girdle muscular dystrophy type 2 6 rec.
                                     |__autosomal dominant limb-girdle muscular dystrophy type 3 5 rec.
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Is a autosomal dominant disease
limb-girdle muscular dystrophy
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Synonyms
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ICD10CM:G71.0
MIM:PS603511
ORDO:102014