complement component 5 deficiency Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_8158)
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19 genes co-occuring with the disease complement component 5 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
C5 complement component 5 2.2915
C5AR1 complement component 5a receptor 1 1.31319
AP2M1 adaptor-related protein complex 2, mu 1 subunit 0.797872
RDH11 retinol dehydrogenase 11 (all-trans/9-cis/11-cis) 0.677105
CR1 complement component (3b/4b) receptor 1 (Knops blood group) 0.669936
C3 complement component 3 0.65763
C1R complement component 1, r subcomponent 0.617877
HIST2H2AC histone cluster 2, H2ac 0.514956
HIST2H2AA3 histone cluster 2, H2aa3 0.514571
HIST2H2AA4 histone cluster 2, H2aa4 0.514571
CFP complement factor properdin 0.512264
CFB complement factor B 0.509576
C4A complement component 4A (Rodgers blood group) 0.434524
NR1H4 nuclear receptor subfamily 1, group H, member 4 0.391513
NPPB natriuretic peptide B 0.332852
CFH complement factor H 0.242945
PIGA phosphatidylinositol glycan anchor biosynthesis, class A 0.241895
PDGFB platelet-derived growth factor beta polypeptide 0.223853
CP ceruloplasmin (ferroxidase) 0.168854