JSON

complement deficiency

^ http://purl.obolibrary.org/obo/MONDO_0003832

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. [ PMID:20930072 PMID:16026838 MONDO:nv ]

Term info

database cross reference
  • ICD9:279.8 (MONDO:relatedTo)
  • SCTID:24743004 (MONDO:equivalentTo)
  • DOID:626 (MONDO:equivalentTo)
  • UMLS:C0272242 (NCIT:C4691)
  • Orphanet:459345 (MONDO:equivalentTo)
  • NCIT:C4691 (MONDO:equivalentTo)
Subsets

disease_grouping, ordo_group_of_disorders

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.

exactMatch

http://purl.obolibrary.org/obo/DOID_626, http://linkedlifedata.com/resource/umls/id/C0272242, http://identifiers.org/snomedct/24743004, http://purl.obolibrary.org/obo/NCIT_C4691, http://purl.obolibrary.org/obo/Orphanet_459345

has exact synonym

complement deficiency, complement activation disease, complement deficiency disease, disorder of complement activation, immunodeficiency due to a complement cascade component deficiency

id

MONDO:0003832