loading...| Preferred Name | complement deficiency | |
| Synonyms |
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 |
|
| alternative label |
Complement deficiency disease |
|
| database_cross_reference |
ICD10CM:D84.1 UMLS_CUI:C0272242 SNOMEDCT_US_2023_03_01:191014008 MESH:D000081208 NCI:C4691 |
|
| 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. |
|
| has exact synonym |
Complement deficiency disease |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:626 |
|
| in_subset | ||
| label |
complement deficiency |
|
| notation |
DOID:626 |
|
| note |
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. |
|
| preferred label |
complement deficiency |
|
| prefLabel |
complement deficiency |
|
| subClassOf |