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ONTOLOGY REPORT - ANNOTATIONS


Term:Gordon Syndrome
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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.


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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
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14759
    syndrome 4210
      Gordon Syndrome 1
Path 2
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  disease 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        Congenital Abnormalities 3137
          Musculoskeletal Abnormalities 1185
            Craniofacial Abnormalities 945
              Maxillofacial Abnormalities 199
                Jaw Abnormalities 196
                  orofacial cleft 108
                    cleft palate 90
                      Gordon Syndrome 1
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