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	melioidosis

Disease ID	1189
Disease	melioidosis
Definition	A disease of humans and animals that resembles GLANDERS. It is caused by BURKHOLDERIA PSEUDOMALLEI and may range from a dormant infection to a condition that causes multiple abscesses, pneumonia, and bacteremia.
Synonym	[x]melioidosis, unspecified [x]melioidosis, unspecified (disorder) infection due to burkholderia pseudomallei infection due to malleomyces pseudomallei infection due to pseudomonas pseudomallei infection due to whitmore's bacillus melioidoses melioidosis (disorder) melioidosis [disease/finding] pseudocholera pseudoglanders pseudoglanders (disorder) stanton disease stanton's disease whitmore disease whitmore's disease
Orphanet	ORPHANET:31202
DOID	DOID:5052
UMLS	C0025229
MeSH	D008554
SNOMED-CT	SNOMEDCT_US_2016_09_01:428111003
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:21) C0032285 \| pneumonia \| 7 C0011847 \| diabetes \| 5 C0029443 \| osteomyelitis \| 3 C0272412 \| splenic abscess \| 2 C0011849 \| diabetes mellitus \| 2 C0014038 \| encephalitis \| 2 C0031039 \| pericardial effusion \| 2 C0520575 \| acute pyelonephritis \| 1 C0039730 \| thalassemia \| 1 C0024205 \| lymphadenitis \| 1 C0032285 \| lung inflammation \| 1 C0014070 \| encephalomyelitis \| 1 C1145670 \| respiratory failure \| 1 C0025289 \| meningitis \| 1 C0004626 \| bacterial pneumonia \| 1 C0018203 \| chronic granulomatous disease \| 1 C0026975 \| myelitis \| 1 C0041327 \| pulmonary tuberculosis \| 1 C0041296 \| tuberculosis \| 1 C0015652 \| fascioliasis \| 1 C0034186 \| pyelonephritis \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:73) 3267 \| AGFG1 \| 1.277 \| DISEASES 1822 \| ATN1 \| 1.27 \| DISEASES 220202 \| ATOH7 \| 1.07 \| DISEASES 64919 \| BCL11B \| 1.626 \| DISEASES 765 \| CA6 \| 2.363 \| DISEASES 766 \| CA7 \| 2.335 \| DISEASES 799 \| CALCR \| 1.1 \| DISEASES 820 \| CAMP \| 2.563 \| DISEASES 834 \| CASP1 \| 2.57 \| DISEASES 959 \| CD40LG \| 3.197 \| DISEASES 8476 \| CDC42BPA \| 2.774 \| DISEASES 1041 \| CDSN \| 1.297 \| DISEASES 4283 \| CXCL9 \| 1.85 \| DISEASES 414325 \| DEFB103A \| 1.331 \| DISEASES 55894 \| DEFB103B \| 1.331 \| DISEASES 100289462 \| DEFB4B \| 1.674 \| DISEASES 10301 \| DLEU1 \| 2.237 \| DISEASES 84062 \| DTNBP1 \| 1.272 \| DISEASES 80153 \| EDC3 \| 3.186 \| DISEASES 1915 \| EEF1A1 \| 1.406 \| DISEASES 84498 \| FAM120B \| 1.428 \| DISEASES 10979 \| FERMT2 \| 1.985 \| DISEASES 2317 \| FLNB \| 1.534 \| DISEASES 2582 \| GALE \| 2.357 \| DISEASES 29933 \| GPR132 \| 2.224 \| DISEASES 3198 \| HOXA1 \| 2.086 \| DISEASES 3329 \| HSPD1 \| 3.038 \| DISEASES 3447 \| IFNA13 \| 2.797 \| DISEASES 3456 \| IFNB1 \| 1.694 \| DISEASES 338376 \| IFNE \| 2.352 \| DISEASES 3586 \| IL10 \| 2.151 \| DISEASES 3605 \| IL17A \| 1.28 \| DISEASES 246778 \| IL27 \| 2.063 \| DISEASES 259307 \| IL4I1 \| 1.511 \| DISEASES 3654 \| IRAK1 \| 1.09 \| DISEASES 9445 \| ITM2B \| 1.198 \| DISEASES 23303 \| KIF13B \| 3.012 \| DISEASES 3850 \| KRT3 \| 1.848 \| DISEASES 3916 \| LAMP1 \| 2.183 \| DISEASES 3996 \| LLGL1 \| 1.397 \| DISEASES 79104 \| MEG8 \| 1.174 \| DISEASES 4600 \| MX2 \| 1.507 \| DISEASES 4601 \| MXI1 \| 2.88 \| DISEASES 4615 \| MYD88 \| 3.158 \| DISEASES 4671 \| NAIP \| 1.335 \| DISEASES 23310 \| NCAPD3 \| 2.933 \| DISEASES 58484 \| NLRC4 \| 3.432 \| DISEASES 114548 \| NLRP3 \| 2.06 \| DISEASES 5074 \| PAWR \| 1.696 \| DISEASES 5100 \| PCDH8 \| 1.984 \| DISEASES 5590 \| PRKCZ \| 1.485 \| DISEASES 5660 \| PSAP \| 2.567 \| DISEASES 5690 \| PSMB2 \| 2.91 \| DISEASES 5696 \| PSMB8 \| 1.355 \| DISEASES 5888 \| RAD51 \| 2.557 \| DISEASES 8437 \| RASAL1 \| 2.179 \| DISEASES 25813 \| SAMM50 \| 3.545 \| DISEASES 23098 \| SARM1 \| 2.758 \| DISEASES 462 \| SERPINC1 \| 1.665 \| DISEASES 5345 \| SERPINF2 \| 1.384 \| DISEASES 6628 \| SNRPB \| 1.292 \| DISEASES 9021 \| SOCS3 \| 1.878 \| DISEASES 26136 \| TES \| 1.258 \| DISEASES 7056 \| THBD \| 1.617 \| DISEASES 7096 \| TLR1 \| 2.926 \| DISEASES 7099 \| TLR4 \| 3.046 \| DISEASES 7100 \| TLR5 \| 3.715 \| DISEASES 10333 \| TLR6 \| 2.234 \| DISEASES 7124 \| TNF \| 3.066 \| DISEASES 7187 \| TRAF3 \| 1.2 \| DISEASES 54209 \| TREM2 \| 1.166 \| DISEASES 706 \| TSPO \| 1.659 \| DISEASES 5212 \| VIT \| 1.686 \| DISEASES
Locus	(Waiting for update.)

Disease ID	1189
Disease	melioidosis
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:18) HP:0100806 \| Sepsis \| 13 HP:0002090 \| Pneumonia \| 8 HP:0002754 \| Bone infection \| 3 HP:0002383 \| Encephalitis \| 2 HP:0000819 \| Diabetes mellitus \| 2 HP:0001698 \| Pericardial effusions \| 2 HP:0002617 \| Aneurysmal dilatation \| 2 HP:0002878 \| Respiratory failure \| 1 HP:0001945 \| Fever \| 1 HP:0001298 \| Encephalopathy \| 1 HP:0012486 \| Inflammation of spinal cord \| 1 HP:0002716 \| Lymph node hyperplasia \| 1 HP:0001287 \| Meningitis \| 1 HP:0100721 \| Mediastinal lymphadenopathy \| 1 HP:0012330 \| Pyelonephritis \| 1 HP:0100523 \| Hepatic abscess \| 1 HP:0002110 \| Bronchiectasis \| 1 HP:0002840 \| Lymphadenitis \| 1

Disease ID	1189
Disease	melioidosis
Manually Symptom	UMLS \| Name(Total Manually Symptoms:14) C2364133 \| infection C2186532 \| liver disease C1963154 \| renal failure C1719672 \| severe sepsis C1550639 \| fistula C1546533 \| abscess C0752303 \| urological manifestations C0685928 \| suppurative parotitis C0264490 \| acute respiratory failure C0263978 \| soft tissue disease C0156290 \| prostatic abscess C0037928 \| spinal cord disease C0037198 \| sinus thrombosis C0023885 \| liver abscesses
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:4) C0009450 \| infection \| 7 C0000833 \| abscess \| 1 C1719672 \| severe sepsis \| 1 C0023885 \| liver abscesses \| 1

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:0)
(Waiting for update.)

GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)

GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)

Mapped by lexical matching(Total Items:0)
(Waiting for update.)

Mapped by homologous gene(Total Items:0)
(Waiting for update.)

Disease ID	1189
Disease	melioidosis
Case	(Waiting for update.)

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