loading...| Preferred Name |
complement deficiency |
|
| Synonyms |
Complement deficiency Complement deficiency disease |
|
| Definitions |
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. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_626 |
|
| database_cross_reference |
SNOMEDCT_US_2020_03_01:191014008 ICD10CM:D84.1 UMLS_CUI:C0272242 MESH:D000081208 NCI:C4691 |
|
| has exact synonym |
Complement deficiency Complement deficiency disease |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:626 |
|
| imported from | ||
| in_subset | ||
| label |
complement deficiency |
|
| notation |
DOID:626 |
|
| prefLabel |
complement deficiency |
|
| textual definition |
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. |
|
| subClassOf |
The BioAssay Ontology integrates with OntoloBridge, allowing community users to suggest additions to the public ontology. Complete the template below to submit a term request directly to the ontology maintainer.
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Example: Involves the use of a tissue derived from a living organism and is a heterogeneous assay type.
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