Mondo Disease Ontology

Last uploaded: November 25, 2024
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

http://linkedlifedata.com/resource/umls/id/C0272242

http://identifiers.org/snomedct/24743004

terms_conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/basis_in_disruption_of_process.yaml

http://purl.obolibrary.org/obo/disrupts_process.yaml

treeView

http://purl.obolibrary.org/obo/MONDO_0003778

http://purl.obolibrary.org/obo/MONDO_0021094

subClassOf

http://purl.obolibrary.org/obo/MONDO_0003778

http://purl.obolibrary.org/obo/MONDO_0021094

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/MONDO_0003832 OBA SAME_URI
http://purl.obolibrary.org/obo/MONDO_0003832 CCONT SAME_URI
http://purl.obolibrary.org/obo/MONDO_0003832 EFO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0003832 DOVES SAME_URI
http://purl.obolibrary.org/obo/MONDO_0003832 KTAO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0003832 OBA LOOM
http://purl.obolibrary.org/obo/MONDO_0003832 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0003832 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0003832 DOVES LOOM
http://purl.obolibrary.org/obo/MONDO_0003832 KTAO LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0272242 OCHV LOOM
http://www.semanticweb.org/ontologies/2012/5/Ontology1338526551855.owl#Complement_Deficiency RPO LOOM
http://purl.bioontology.org/ontology/RCD/X20Hs RCD LOOM
http://www.phoc.org.cn/pmo/class/PMO_00008535 PMAPP-PMO LOOM
http://purl.obolibrary.org/obo/NCIT_C4691 BERO LOOM
http://purl.jp/bio/4/id/200906048634667830 IOBC LOOM
http://purl.obolibrary.org/obo/DOID_626 DTO LOOM
http://purl.obolibrary.org/obo/DOID_626 DOID LOOM
http://purl.obolibrary.org/obo/DOID_626 BAO LOOM
http://purl.obolibrary.org/obo/DOID_626 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_626 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_626 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_626 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_626 FNS-H LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_626 NATPRO LOOM
http://purl.bioontology.org/ontology/CSP/1560-6347 CRISP LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C4691 NCIT LOOM
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:2253 IFAR LOOM