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ONTOLOGY REPORT - ANNOTATIONS


Term:polycystic kidney disease 5
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Accession:DOID:0080273 term browser browse the term
Definition:A form of autosomal recessive polycystic kidney disease (ARPKD), that is characterized by early childhood onset of progressive renal dysfunction associated with enlarged hyperechogenic kidneys that often results in end-stage renal disease in the second or third decade of life. Arterial hypertension is apparent in early childhood. (OMIM)
Synonyms:exact_synonym: PKD5
 primary_id: OMIM:617610
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polycystic kidney disease 5 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dzip1l DAZ interacting zinc finger protein 1-like JBrowse link 8 107,875,659 107,916,298 RGD:8554872
RGD:7240710

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Path 1
Term Annotations click to browse term
  disease 16021
    Developmental Diseases 9337
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8165
        genetic disease 7689
          polycystic kidney disease 109
            autosomal recessive polycystic kidney disease 40
              polycystic kidney disease 5 1
Path 2
Term Annotations click to browse term
  disease 16021
    Developmental Diseases 9337
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8165
        genetic disease 7689
          monogenic disease 5447
            autosomal genetic disease 4411
              autosomal recessive disease 2386
                autosomal recessive polycystic kidney disease 40
                  polycystic kidney disease 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.