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Term:Properdin Deficiency, Type III
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Accession:DOID:9005460 term browser browse the term
Synonyms:primary_id: MESH:C564076;   RDO:0013157
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Properdin Deficiency, Type III term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cfp complement factor properdin JBrowse link X 1,311,121 1,316,683 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15043
    syndrome 4811
      primary immunodeficiency disease 930
        Properdin Deficiency, Type III 1
Path 2
Term Annotations click to browse term
  disease 15043
    Developmental Diseases 7871
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7202
        genetic disease 6577
          monogenic disease 3292
            X-linked monogenic disease 837
              Properdin Deficiency, Type III 1
paths to the root


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