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immunodeficiency due to a classical component pathway complement deficiency - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

immunodeficiency due to a classical component pathway complement deficiency

MONDO:0015699

Also known as:immunodeficiency due to C1, C4, or C2 component complement deficiencyimmunodeficiency due to a C1, C4, or C2 component complement deficiencyimmunodeficiency due to an early component of complement deficiency

Overview

OnsetINFANTILE, CHILDHOOD

Diagnosis

Biomarker and diagnostic research for immunodeficiency due to a classical component pathway complement deficiency has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for immunodeficiency due to a classical component pathway complement deficiency.

25 publications have been identified in PubMed for immunodeficiency due to a classical component pathway complement deficiency. Research spans Case Report / Case Series (32%), Review / Meta-Analysis (28%), and Epidemiology / Natural History (24%).

Research Type	Count	% of Total
Patient case studies	8	32%

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 6:53 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:169147

GARD

Genetic and Rare Diseases Info Center

GARD:15025

Questions for Your Care Team

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immunodeficiency due to a classical component pathway complement deficiency

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications