african trypanosomiasis |
Disease ID | 784 |
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Disease | african trypanosomiasis |
Definition | A disease endemic among people and animals in Central Africa. It is caused by various species of trypanosomes, particularly T. gambiense and T. rhodesiense. Its second host is the TSETSE FLY. Involvement of the central nervous system produces "African sleeping sickness." Nagana is a rapidly fatal trypanosomiasis of horses and other animals. |
Synonym | [x]african trypanosomiasis, unspecified [x]african trypanosomiasis, unspecified (disorder) african sickness sleeping african sleeping sickness african sleeping sicknesses african trypanosoma nos african trypanosomiases african trypanosomiasis (disorder) african trypanosomiasis nos african trypanosomiasis nos (disorder) african trypanosomiasis, unspecified maladie du sommeil schlafkrankheit sickness sleeping sickness, african sleeping sicknesses, african sleeping sleeping sickness sleeping sickness nos sleeping sickness, african sleeping sickness, nos sleeping sicknesses, african trypanosomiases, african trypanosomiasis, african trypanosomiasis, african [disease/finding] |
Orphanet | |
DOID | |
ICD10 | |
UMLS | C0041228 |
MeSH | |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:9) C0041228 | african sleeping sickness | 31 C0041227 | trypanosomiasis | 5 C0024530 | malaria | 1 C0011881 | diabetic kidney disease | 1 C0041228 | sleeping sickness | 1 C0235618 | proliferative glomerulonephritis | 1 C0041234 | chagas disease | 1 C0022658 | kidney disease | 1 C0017662 | membranoproliferative glomerulonephritis | 1 |
Curated Gene | (Waiting for update.) |
Inferring Gene | Entrez_id | Symbol | Resource(Total Genes:2) |
Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:122) 50808 | AK3 | 2.358 | DISEASES 205 | AK4 | 1.954 | DISEASES 501 | ALDH7A1 | 1.731 | DISEASES 262 | AMD1 | 3.991 | DISEASES 60489 | APOBEC3G | 1.198 | DISEASES 522 | ATP5J | 1.358 | DISEASES 7917 | BAG6 | 2.044 | DISEASES 57545 | CC2D2A | 1.969 | DISEASES 911 | CD1C | 1.315 | DISEASES 912 | CD1D | 1.418 | DISEASES 344807 | CD200R1L | 3.608 | DISEASES 51744 | CD244 | 1.461 | DISEASES 959 | CD40LG | 3.718 | DISEASES 8760 | CDS2 | 2.967 | DISEASES 85301 | COL27A1 | 3.669 | DISEASES 8532 | CPZ | 4.014 | DISEASES 1503 | CTPS1 | 2.182 | DISEASES 1506 | CTRL | 1.417 | DISEASES 1508 | CTSB | 3.109 | DISEASES 8454 | CUL1 | 1.018 | DISEASES 9937 | DCLRE1A | 1.932 | DISEASES 23564 | DDAH2 | 1.279 | DISEASES 196385 | DNAH10 | 3.434 | DISEASES 1759 | DNM1 | 1.102 | DISEASES 1785 | DNM2 | 1.097 | DISEASES 9732 | DOCK4 | 2.053 | DISEASES 124454 | EARS2 | 1.463 | DISEASES 1984 | EIF5A | 1.686 | DISEASES 2013 | EMP2 | 1.621 | DISEASES 377841 | ENTPD8 | 2.193 | DISEASES 132884 | EVC2 | 1.213 | DISEASES 2170 | FABP3 | 1.322 | DISEASES 2224 | FDPS | 2.688 | DISEASES 342184 | FMN1 | 1.144 | DISEASES 2582 | GALE | 2.951 | DISEASES 26301 | GBGT1 | 1.773 | DISEASES 2710 | GK | 1.54 | DISEASES 51022 | GLRX2 | 3.001 | DISEASES 8833 | GMPS | 1.51 | DISEASES 2804 | GOLGB1 | 1.062 | DISEASES 2821 | GPI | 1.012 | DISEASES 2959 | GTF2B | 1.536 | DISEASES 3005 | H1F0 | 2.063 | DISEASES 3098 | HK1 | 2.604 | DISEASES 3135 | HLA-G | 1.392 | DISEASES 3240 | HP | 3.343 | DISEASES 3250 | HPR | 5.406 | DISEASES 3320 | HSP90AA1 | 1.957 | DISEASES 3586 | IL10 | 2.839 | DISEASES 253430 | IPMK | 2.156 | DISEASES 3652 | IPP | 1.087 | DISEASES 51477 | ISYNA1 | 3.368 | DISEASES 8564 | KMO | 1.489 | DISEASES 51520 | LARS | 1.87 | DISEASES 3963 | LGALS7 | 1.644 | DISEASES 225689 | MAPK15 | 4.138 | DISEASES 4190 | MDH1 | 1.781 | DISEASES 4199 | ME1 | 2.026 | DISEASES 57496 | MKL2 | 2.097 | DISEASES 54903 | MKS1 | 1.979 | DISEASES 4512 | MT-CO1 | 2.053 | DISEASES 4519 | MT-CYB | 1.406 | DISEASES 4536 | MT-ND2 | 1.99 | DISEASES 26151 | NAT9 | 1.735 | DISEASES 58484 | NLRC4 | 2.31 | DISEASES 4843 | NOS2 | 1.758 | DISEASES 594857 | NPS | 1.334 | DISEASES 4905 | NSF | 1.002 | DISEASES 4923 | NTSR1 | 2.632 | DISEASES 8481 | OFD1 | 1.516 | DISEASES 164091 | PAQR7 | 3.136 | DISEASES 5144 | PDE4D | 2.034 | DISEASES 10026 | PIGK | 3.035 | DISEASES 9033 | PKD2L1 | 1.768 | DISEASES 11201 | POLI | 3.429 | DISEASES 5464 | PPA1 | 2.669 | DISEASES 5550 | PREP | 1.325 | DISEASES 58155 | PTBP2 | 1.598 | DISEASES 5770 | PTPN1 | 1.059 | DISEASES 8480 | RAE1 | 2.691 | DISEASES 57038 | RARS2 | 1.958 | DISEASES 1104 | RCC1 | 1.433 | DISEASES 7955 | RNF217-AS1 | 2.328 | DISEASES 6135 | RPL11 | 1.541 | DISEASES 6207 | RPS13 | 1.133 | DISEASES 6319 | SCD | 1.294 | DISEASES 11231 | SEC63 | 2.081 | DISEASES 6906 | SERPINA7 | 2.471 | DISEASES 6418 | SET | 1.472 | DISEASES 6580 | SLC22A1 | 1.194 | DISEASES 10478 | SLC25A17 | 1.323 | DISEASES 91137 | SLC25A46 | 1.52 | DISEASES 113235 | SLC46A1 | 1.519 | DISEASES 6594 | SMARCA1 | 2.675 | DISEASES 26806 | SNORD44 | 2.126 | DISEASES 200162 | SPAG17 | 1.513 | DISEASES 9576 | SPAG6 | 2.173 | DISEASES 6723 | SRM | 4.001 | DISEASES 10250 | SRRM1 | 1.708 | DISEASES 8428 | STK24 | 1.111 | DISEASES 6863 | TAC1 | 1.22 | DISEASES 80222 | TARS2 | 2.03 | DISEASES 123283 | TARSL2 | 2.067 | DISEASES 55171 | TBCCD1 | 3.764 | DISEASES 10716 | TBR1 | 3.294 | DISEASES 84066 | TEX35 | 3.444 | DISEASES 7018 | TF | 2.793 | DISEASES 7037 | TFRC | 1.518 | DISEASES 8914 | TIMELESS | 1.69 | DISEASES 10440 | TIMM17A | 3.718 | DISEASES 7124 | TNF | 2.853 | DISEASES 51592 | TRIM33 | 2.022 | DISEASES 5756 | TWF1 | 3.621 | DISEASES 7295 | TXN | 1.008 | DISEASES 7306 | TYRP1 | 1.486 | DISEASES 51271 | UBAP1 | 1.295 | DISEASES 2837 | UTS2R | 1.644 | DISEASES 57176 | VARS2 | 2.273 | DISEASES 6944 | VPS72 | 2.223 | DISEASES 23038 | WDTC1 | 2.725 | DISEASES 79971 | WLS | 1.41 | DISEASES 9278 | ZBTB22 | 1.036 | DISEASES |
Locus | (Waiting for update.) |
Disease ID | 784 |
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Disease | african trypanosomiasis |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:3) |
Disease ID | 784 |
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Disease | african trypanosomiasis |
Manually Symptom | UMLS | Name(Total Manually Symptoms:13) C2364072 | depression C1963101 | encephalopathy C1373218 | immunosuppression C1000483 | anemia C0752303 | urological manifestations C0476270 | cardiovascular symptoms C0348024 | thyroid dysfunction C0085584 | encephalopathies C0038454 | stroke C0026976 | transverse myelitis C0021053 | immune dysfunction C0014038 | encephalitis C0002871 | anaemia |
Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:3) |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
Text Mining Genotype(Total Genotypes:0) | |
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(Waiting for update.) |
All Snps(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Annotation(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Snp Trait(Total Genotypes:0) | |
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(Waiting for update.) |
Mapped by lexical matching(Total Items:0) |
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(Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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(Waiting for update.) |
Disease ID | 784 |
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Disease | african trypanosomiasis |
Case | (Waiting for update.) |