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ONTOLOGY REPORT - ANNOTATIONS


Term:focal segmental glomerulosclerosis 5
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Accession:DOID:0111130 term browser browse the term
Definition:A focal segmental glomerulosclerosis that has_material_basis_in an autosomal dominant mutation of INF2 on chromosome 14q32.33. (DO)
Synonyms:exact_synonym: FSGS5
 primary_id: MESH:C567687
 alt_id: OMIM:613237;   RDO:0015692
For additional species annotation, visit the Alliance of Genome Resources.


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focal segmental glomerulosclerosis 5 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Inf2 inverted formin, FH2 and WH2 domain containing JBrowse link 6 137,162,593 137,180,198 RGD:7240710
RGD:8554872

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Term Annotations click to browse term
  disease 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        genetic disease 5913
          focal segmental glomerulosclerosis 5 1
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      Urogenital Diseases 3755
        urinary system disease 1990
          kidney disease 1786
            nephritis 412
              glomerulonephritis 359
                glomerulosclerosis 119
                  focal segmental glomerulosclerosis 105
                    focal segmental glomerulosclerosis 5 1
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