FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term distal arthrogryposis type 1A ID (Ontology) DOID:0111597 (Human Disease)
Definition A distal arthrogryposis type 1 that has_material_basis_in heterozygous mutation in the TPM2 gene on chromosome 9p13.3.
Also Known As "DA1A"
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DO.org
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Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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Relevant FlyBase reports
 Genes Human Disease Models
 distal arthrogryposis type 1A       3      1
 for disease ribbon | distal arthrogryposis type 1A       2       --
 model of | distal arthrogryposis type 1A       2       --
Spanning Tree (Parents/Children)
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distal arthrogryposis
 |__distal arthrogryposis type 1__
autosomal genetic disease         |
 |__autosomal dominant disease____|
                                  distal arthrogryposis type 1A  4 rec.
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Is a autosomal dominant disease
distal arthrogryposis type 1
Part of
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Synonyms
  • "DA1A" EXACT OMO:0003012
Secondary IDs
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MESH:C535378
MIM:108120