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Term:TARP Syndrome
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Accession:DOID:9005152 term browser browse the term
Definition:TARP syndrome is caused by hemizygous mutation in the RBM10 gene on chromosome Xp11. (OMIM)
Synonyms:exact_synonym: Pierre Robin syndrome with congenital heart malformation and clubfoot;   TARPS;   Talipes Equinovarus, Atrial Septal Defect, Robin Sequence, and Persistence of Left Superior Vena Cava
 primary_id: MESH:C536942;   RDO:0002670
 alt_id: OMIM:311900
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TARP Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rbm10 RNA binding motif protein 10 JBrowse link X 1,754,869 1,786,973 RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15553
    syndrome 5224
      TARP Syndrome 1
Path 2
Term Annotations click to browse term
  disease 15553
    Developmental Diseases 8823
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7613
        Congenital Abnormalities 3730
          Musculoskeletal Abnormalities 1340
            Congenital Limb Deformities 413
              Lower Extremity Deformities, Congenital 75
                Congenital Foot Deformities 67
                  Talipes 40
                    clubfoot 30
                      TARP Syndrome 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.