Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

ONTOLOGY REPORT - ANNOTATIONS


Term:Properdin Deficiency, Type III
go back to main search page
Accession:DOID:9005460 term browser browse the term
Synonyms:primary_id: MESH:C564076;   RDO:0013157
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 
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

NHLBI Logo

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