Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   


Term:Gordon Syndrome
go back to main search page
Accession:DOID:9001612 term browser browse the term
Synonyms:exact_synonym: Arthrogryposis Multiplex Congenita, Distal, Type IIa;   Arthrogryposis multiplex congenita, distal, type 2a;   Camptodactyly, cleft palate, and clubfoot;   DA3;   Distal arthrogryposis, type 3
 primary_id: MESH:C537288;   OMIM:114300;   RDO:0003103
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants       view all columns           Sort by:
Gordon Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Piezo2 piezo-type mechanosensitive ion channel component 2 JBrowse link 18 58,353,361 58,728,555 RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15603
    syndrome 5215
      Gordon Syndrome 1
Path 2
Term Annotations click to browse term
  disease 15603
    Developmental Diseases 8772
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7555
        Congenital Abnormalities 3620
          Musculoskeletal Abnormalities 1313
            Congenital Limb Deformities 413
              Lower Extremity Deformities, Congenital 76
                Congenital Foot Deformities 68
                  Talipes 41
                    clubfoot 31
                      Gordon Syndrome 1
paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.