RGD DISEASE ONTOLOGY - ANNOTATIONS
RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term: Plasmodium falciparum malaria
Accession: DOID:14067
browse the term
Definition: A malaria described as a severe form of the disease caused by a parasite Plasmodium falciparum, which is marked by irrregular recurrence of paroxysms and prolonged or continuous fever. (DO)
Synonyms: exact_synonym: falciparum malaria; malaria fever, subtertian; malignant tertian fever
primary_id: MESH:D016778
xref: EFO:0007444 ; ICD10CM:B50 ; ICD9CM:084.0 ; NCI:C34798
For additional species annotation, visit the
Alliance of Genome Resources .
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G
ABO
ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase
susceptibility
ISO
DNA:SNPs,haplotype:multiple
RGD
PMID:18003641
RGD:39938831
NCBI chr12:4,863,100...4,892,204
Ensembl chr12:4,863,165...4,885,849
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ADAMTS13
ADAM metallopeptidase with thrombospondin type 1 motif 13
ISO
protein:decreased activity:plasma (human)
RGD
PMID:20062916
RGD:10449041
NCBI chr12:4,677,237...4,718,825
Ensembl chr12:4,677,229...4,714,386
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BSG
basigin (Ok blood group)
ISO
CTD Direct Evidence: therapeutic
CTD
PMID:22080952 PMID:26195724
NCBI chr 6:309,579...320,209
Ensembl chr 6:309,506...321,785
G
CAST
calpastatin
ISO
protein:alter localization:erythrocyte
RGD
PMID:17359359
RGD:5509812
NCBI chr 4:90,496,867...90,607,019
Ensembl chr 4:90,497,754...90,605,481
G
CLEC11A
C-type lectin domain containing 11A
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:19884328
NCBI chr 6:43,780,151...43,782,780
G
CR1
complement C3b/C4b receptor 1 (Knops blood group)
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:9230440 PMID:11724985
NCBI chr25:21,787,237...21,909,462
G
CYP2C19
cytochrome P450 family 2 subfamily C member 19
treatment
ISO
DNA:polymorphisms::
RGD
PMID:10471063
RGD:124713538
NCBI chr 9:87,981,300...88,025,007
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FCGR2A
Fc fragment of IgG receptor IIa
severity
ISO
DNA:missense mutation:cds:p.R131H (rs1801274) (human)
RGD
PMID:18194515
RGD:5147927
NCBI chr20:2,480,710...2,512,429
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G6PD
glucose-6-phosphate dehydrogenase
severity
ISO
DNA:missense mutation:cds:202G>A (p.V68M) (human)
RGD
PMID:24943486
RGD:10449113
NCBI chr X:128,768,028...128,788,366
Ensembl chr X:128,770,268...128,786,961
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GSTP1
glutathione S-transferase pi 1
severity
ISO
RGD
PMID:19635899
RGD:10450848
NCBI chr 1:6,676,897...6,679,936
G
IL13
interleukin 13
ISO
protein:increased expression:plasma
RGD
PMID:21985368
RGD:5684362
NCBI chr23:35,475,762...35,479,419
Ensembl chr23:35,476,490...35,478,869
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MBL2
mannose binding lectin 2
susceptibility
ISO
DNA:haplotype:exon:
RGD
PMID:18396436
RGD:11530064
NCBI chr 9:78,389,534...78,394,753
Ensembl chr 9:78,389,947...78,396,079
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TNF
tumor necrosis factor
severity
ISO
protein:increased expression:plasma
RGD
PMID:1984482
RGD:10450571
G
IL10
interleukin 10
ISO
RGD
PMID:24717969
RGD:11041890
NCBI chr25:22,590,389...22,595,877
Ensembl chr25:22,590,962...22,594,836
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