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ONTOLOGY REPORT - ANNOTATIONS


Term:Galloway-Mowat syndrome 2
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Accession:DOID:0080244 term browser browse the term
Synonyms:exact_synonym: GAMOS2;   Galloway-Mowat syndrome 2, X-linked
 primary_id: OMIM:301006
 alt_id: RDO:9005164
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Galloway-Mowat syndrome 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Lage3 L antigen family, member 3 JBrowse link X 156,355,376 156,356,799 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15619
    syndrome 5154
      Galloway-Mowat syndrome 9
        Galloway-Mowat syndrome 2 1
Path 2
Term Annotations click to browse term
  disease 15619
    Developmental Diseases 8737
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7519
        genetic disease 7008
          monogenic disease 4561
            autosomal genetic disease 3515
              autosomal dominant disease 2079
                complex cortical dysplasia with other brain malformations 481
                  Malformations of Cortical Development, Group I 338
                    microcephaly 210
                      Galloway-Mowat syndrome 9
                        Galloway-Mowat syndrome 2 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.