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 |
|
database_cross_reference |
DOID:626 Orphanet:459345 NANDO:2200776 UMLS:C0272242 NCIT:C4691 NANDO:1200364 MEDGEN:82898 ICD9:279.8 SCTID:24743004 |
|
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. |
|
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 |
|
in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-simple#otar http://purl.obolibrary.org/obo/mondo/mondo-simple#ordo_group_of_disorders http://purl.obolibrary.org/obo/mondo/mondo-simple#rare http://purl.obolibrary.org/obo/mondo/mondo-simple#disease_grouping http://purl.obolibrary.org/obo/mondo/mondo-simple#inferred_rare |
|
label |
complement deficiency |
|
notation |
MONDO:0003832 |
|
prefLabel |
complement deficiency |
|
skos_exactMatch |
http://identifiers.org/medgen/82898 http://purl.obolibrary.org/obo/Orphanet_459345 http://purl.obolibrary.org/obo/NCIT_C4691 http://purl.obolibrary.org/obo/DOID_626 |
|
terms_conformsTo |
http://purl.obolibrary.org/obo/mondo/patterns/basis_in_disruption_of_process.yaml |
|
treeView | ||
subClassOf |