loading...| Preferred Name |
complement deficiency |
|
| Synonyms |
disorder of complement activation complement deficiency complement deficiency disease immunodeficiency due to a complement cascade component deficiency complement activation disease |
|
| Definitions |
A genetic deficiency of any of the component of the complement system (including the classical, alternative, and terminal pathway components), that can either be acquired or inherited. |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0003832 |
|
| closeMatch | ||
| conformsTo |
http://purl.obolibrary.org/obo/mondo/patterns/basis_in_disruption_of_process.yaml http://purl.obolibrary.org/obo/mondo/patterns/disrupts_process.yaml |
|
| database_cross_reference |
DOID:626 Orphanet:459345 UMLS:C0272242 ICD10:D80-D89 NCIT:C4691 ICD9:279.8 ICD10:D84.1 SCTID:24743004 |
|
| disease has basis in disruption of | ||
| exactMatch |
http://www.orpha.net/ORDO/Orphanet_459345 http://purl.obolibrary.org/obo/NCIT_C4691 http://purl.obolibrary.org/obo/DOID_626 |
|
| has exact synonym |
disorder of complement activation complement deficiency complement deficiency disease immunodeficiency due to a complement cascade component deficiency complement activation disease |
|
| id |
MONDO:0003832 |
|
| imported from | ||
| in_subset |
http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_group_of_disorders |
|
| label |
complement deficiency |
|
| notation |
MONDO:0003832 |
|
| prefLabel |
complement deficiency |
|
| textual definition |
A genetic deficiency of any of the component of the complement system (including the classical, alternative, and terminal pathway components), that can either be acquired or inherited. |
|
| subClassOf |
http://purl.obolibrary.org/obo/MONDO_0000001 |