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
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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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  disease 14926
    Developmental Diseases 7774
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7096
        genetic disease 6457
          focal segmental glomerulosclerosis 5 1
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Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14092
      Urogenital Diseases 3915
        urinary system disease 2015
          kidney disease 1809
            nephritis 412
              glomerulonephritis 359
                glomerulosclerosis 119
                  focal segmental glomerulosclerosis 105
                    focal segmental glomerulosclerosis 5 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.