FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Larsen syndrome ID (Ontology) DOID:14764 (Human Disease)
Definition A syndrome that is characterized by autosomal dominant inheritance of large-joint dislocations and characteristic craniofacial abnormalities.
Also Known As "dominant larsen syndrome"
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DO.org
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 Genes
 Larsen syndrome       3
 for disease ribbon | Larsen syndrome       3
 model of | Larsen syndrome       3
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
disease                         |
 |__syndrome____________________|
                                Larsen syndrome  3 rec.
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Is a autosomal dominant disease
syndrome
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Synonyms
  • "dominant larsen syndrome" EXACT
Secondary IDs
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GARD:6860
MESH:C580241
MIM:150250