Kidney Tissue Atlas Ontology

Last uploaded: March 16, 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

closeMatch

http://identifiers.org/snomedct/191014008

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 causes disruption of

http://purl.obolibrary.org/obo/GO_0006956

disease has basis in disruption of

http://purl.obolibrary.org/obo/GO_0006956

exactMatch

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

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

http://purl.obolibrary.org/obo/mondo.owl

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

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

http://purl.obolibrary.org/obo/MONDO_0015136

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Delete Mapping To Ontology Source
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 MONDO 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 OBA SAME_URI
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 MONDO 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 OBA 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