complement deficiency
Information
- Disease name
- complement deficiency
- Disease ID
- DOID:626
- Description
- "A primary immunodeficiency disease that is the result in a mutation of a gene encoding one of the thirty complement system proteins, produced predominantly in liver, which function to defend against infection and produce inflammation." [url:http\://en.wikipedia.org/wiki/Complement_deficiency]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT02972281 | Terminated | N/A | Systematic Search for Primary Immunodeficiency in Adults With Infections | March 2015 | March 2020 |
- Disase is a (Disease Ontology)
- DOID:612
- Cross Reference ID (Disease Ontology)
- ICD10CM:D84.1
- Cross Reference ID (Disease Ontology)
- MESH:D000081208
- Cross Reference ID (Disease Ontology)
- NCI:C4691
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:191014008
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0272242
- Exact Synonym (Disease Ontology)
- Complement deficiency disease
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0004431