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rare disease where complement protein(s) are absent or in diminished amount relative to the normal requirement of an organism; associated with autoimmune disease or increased susceptibility to infections, problems encountered depend on which pathway is affected.

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Data Correlations | 1 study

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Genes category icon Genes
Score Help
C6 100 100
C1S 95 95
C1R 94 94
C8A 89 89
C9 89 89
C8B 89 89
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Biogroups category icon Biogroups
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Complement and Coagulation Cascades 100 100
Complement Pathway 100 100
Alternative Complement Pathway 99 99
Low density lipoprotein-receptor, c… 96 96
Sushi/SCR/CCP 95 95
Complement control module 94 94
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Individual Studies

  • OMIM - Unspecified immunity deficiency

    Homo sapiens Homo sapiens | Mutations/Phenotypic   Mutations/Phenotypic

    This study contains curated human phenotype data extracted from OMIM. Additional computational processing and curation of the phenotype data was performed to further organize and group data from related phenotypes into unifying disease categories.

    Source: NextBio Library/Mutation and Phenotypic data
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Associated Researchers

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Thought leaders and organizations working on research involving complement deficiency.

View All Author iconAuthors
  • Lennart Truedsson
  • A G Sjöholm
  • Anders G Sjöholm
  • Jeremy S Brown
  • L Truedsson
View All Clinical trial sponsors icon Clinical Trials Sponsors
  • National Heart, Lung, and Blood Institute (NHLBI)
  • Alexion Pharmaceuticals
  • National Cancer Institute (NCI)
  • University of Utah
  • Cubist Pharmaceuticals
View All Affiliations icon Organizations
  • Lund University
  • Imperial College
  • Imperial College London
  • University of California
  • Leiden University Medical Center

Clinical Trials | 47 trials

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Community

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