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 .
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 chr 9:104,354,115...104,399,057
Ensembl chr 9:132,989,574...133,010,324
G
ADAMTS13
ADAM metallopeptidase with thrombospondin type 1 motif 13
ISO
protein:decreased activity:plasma (human)
RGD
PMID:20062916
RGD:10449041
NCBI chr 9:104,541,051...104,582,574
Ensembl chr 9:133,156,761...133,193,707
G
BSG
basigin (Ok blood group)
ISO
CTD Direct Evidence: therapeutic
CTD
PMID:22080952 PMID:26195724
Ensembl chr19:539,815...551,456
G
CAST
calpastatin
ISO
protein:alter localization:erythrocyte
RGD
PMID:17359359
RGD:5509812
NCBI chr 5:91,972,572...92,084,657
Ensembl chr 5:97,527,071...97,636,650
G
CLEC11A
C-type lectin domain containing 11A
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:19884328
NCBI chr19:47,682,806...47,690,389
Ensembl chr19:56,586,183...56,588,580
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CR1
complement C3b/C4b receptor 1 (Knops blood group)
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:9230440 PMID:11724985
NCBI chr 1:183,094,601...183,246,957
G
CYP2C19
cytochrome P450 family 2 subfamily C member 19
treatment
ISO
DNA:polymorphisms::
RGD
PMID:10471063
RGD:124713538
NCBI chr10:91,375,255...91,465,215
Ensembl chr10:94,884,472...94,970,065
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FAS
Fas cell surface death receptor
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:21625619
NCBI chr10:85,707,457...85,741,539
Ensembl chr10:89,217,949...89,243,612
G
G6PD
glucose-6-phosphate dehydrogenase
severity
ISO
DNA:missense mutation:cds:202G>A (p.V68M) (human)
RGD
PMID:24943486
RGD:10449113
NCBI chr X:143,972,798...143,988,960
Ensembl chr X:153,843,092...153,860,674
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GSTP1
glutathione S-transferase pi 1
severity
ISO
RGD
PMID:19635899
RGD:10450848
NCBI chr11:62,942,756...62,945,701
Ensembl chr11:66,253,421...66,256,472
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IL13
interleukin 13
ISO
protein:increased expression:plasma
RGD
PMID:21985368
RGD:5684362
NCBI chr 5:128,073,863...128,078,453
Ensembl chr 5:134,235,788...134,240,548
G
LOC100972994
HLA class II histocompatibility antigen, DQ beta 1 chain
susceptibility
ISO
DNA:polymorphism:cds:HLA-DQB1*0501 (human)
RGD
PMID:11076705
RGD:11041780
NCBI chr 6:32,237,395...32,244,201
Ensembl chr 6:33,353,599...33,360,272
G
LOC100991644
low affinity immunoglobulin gamma Fc region receptor II-a
severity
ISO
DNA:missense mutation:cds:p.R131H (rs1801274) (human)
RGD
PMID:18194515
RGD:5147927
NCBI chr 1:136,892,311...136,906,450
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MBL2
mannose binding lectin 2
susceptibility
ISO
DNA:haplotype:exon:
RGD
PMID:18396436
RGD:11530064
NCBI chr10:49,401,364...49,409,328
Ensembl chr10:51,527,758...51,543,432
G
TNF
tumor necrosis factor
severity
ISO
protein:increased expression:plasma
RGD
PMID:1984482
RGD:10450571
NCBI chr 6:31,236,650...31,239,423
Ensembl chr 6:32,126,618...32,129,381
G
IL10
interleukin 10
ISO
RGD
PMID:24717969
RGD:11041890
NCBI chr 1:182,369,234...182,374,207
Ensembl chr 1:186,648,289...186,653,371
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