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ONTOLOGY REPORT - ANNOTATIONS


Term:Raine Syndrome
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Accession:DOID:9000666 term browser browse the term
Synonyms:exact_synonym: Lethal osteosclerotic bone dysplasia;   RNS
 primary_id: MESH:C535282;   RDO:0000277
 alt_id: OMIM:259775
For additional species annotation, visit the Alliance of Genome Resources.


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Raine Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fam20c FAM20C, golgi associated secretory pathway kinase JBrowse link 12 17,913,771 17,972,733 RGD:7240710
RGD:8554872
RGD:11560486

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15590
    syndrome 5131
      Raine Syndrome 1
Path 2
Term Annotations click to browse term
  disease 15590
    Developmental Diseases 8723
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7503
        genetic disease 6993
          monogenic disease 4551
            autosomal genetic disease 3501
              autosomal dominant disease 2065
                complex cortical dysplasia with other brain malformations 477
                  Malformations of Cortical Development, Group I 334
                    microcephaly 206
                      Raine Syndrome 1
paths to the root

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