JSON

complement deficiency

Go to external page 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. [ http://www.ncbi.nlm.nih.gov/pubmed/20930072 http://www.ncbi.nlm.nih.gov/pubmed/16026838 MONDO:nv ]

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

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:279.8 (MONDO:relatedTo)
  • Orphanet:459345 (MONDO:equivalentTo)
  • UMLS:C0272242 (NCIT:C4691)
  • SCTID:24743004 (MONDO:equivalentTo)
  • NCIT:C4691 (MONDO:equivalentTo)
  • DOID:626 (MONDO:equivalentTo)
  • GARD:21919 (Orphanet:459345)
Subsets

gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders

exactMatch

http://www.orpha.net/ORDO/Orphanet_459345

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

id

MONDO:0003832