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
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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
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  disease 14823
    syndrome 4218
      Gordon Syndrome 1
Path 2
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  disease 14823
    Developmental Diseases 7637
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6675
        Congenital Abnormalities 3149
          Musculoskeletal Abnormalities 1191
            Craniofacial Abnormalities 949
              Maxillofacial Abnormalities 199
                Jaw Abnormalities 196
                  orofacial cleft 108
                    cleft palate 90
                      Gordon 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.