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encyclopedia of Rare Disease Annotation for Precision Medicine

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	amebiasis

Disease ID	1390
Disease	amebiasis
Definition	Infection with any of various amebae. It is an asymptomatic carrier state in most individuals, but diseases ranging from chronic, mild diarrhea to fulminant dysentery may occur.
Synonym	[x]amebiasis, unspecified [x]amebiasis, unspecified (disorder) [x]amoebiasis, unspecified amebiases amebiasis (disorder) amebiasis [disease/finding] amebiasis nos amebiasis nos (disorder) amebiasis, unspecified amebic infection amebic infection (disorder) amoebiases amoebiasis amoebiasis (disorder) amoebiasis nos amoebic infection amoebic infection (disorder) disease caused by endamoebidae disease caused by endamoebidae (disorder) disease due to endamoebidae disease due to endamoebidae (disorder) entamoeba histolytica infection infection caused by entamoeba histolytica infection caused by entamoeba histolytica (disorder) infection due to entameba histolytica infection due to entameba histolytica, sai infection due to entamoeba histolytica infection due to entamoeba histolytica (disorder) infection due to entamoeba histolytica, sai
DOID	DOID:9181
ICD10	ICD10CM:A06.9
UMLS	C0002438
MeSH	D000562
SNOMED-CT	SNOMEDCT_US_2016_09_01:388759003;SNOMEDCT_US_2016_09_01:105637008;SNOMEDCT_US_2016_09_01:111910009
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:13) C0009319 \| colitis \| 4 C0002438 \| amebiasis \| 1 C0020295 \| hydronephrosis \| 1 C0020538 \| hypertension \| 1 C0013370 \| amebic colitis \| 1 C0001175 \| acquired immunodeficiency syndrome (aids) \| 1 C0034152 \| henoch-schonlein purpura \| 1 C0747256 \| parasitic infection \| 1 C0013369 \| dysentery \| 1 C0001175 \| acquired immunodeficiency syndrome \| 1 C0031542 \| phlebitis \| 1 C0013371 \| shigellosis \| 1 C0011991 \| diarrhea \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:85) 55 \| ACPP \| 1.344 \| DISEASES 10097 \| ACTR2 \| 2.067 \| DISEASES 51390 \| AIG1 \| 3.523 \| DISEASES 84335 \| AKT1S1 \| 2.496 \| DISEASES 64400 \| AKTIP \| 1.206 \| DISEASES 279 \| AMY2A \| 1.26 \| DISEASES 9531 \| BAG3 \| 1.26 \| DISEASES 114899 \| C1QTNF3 \| 1.393 \| DISEASES 801 \| CALM1 \| 2.377 \| DISEASES 834 \| CASP1 \| 1.521 \| DISEASES 6364 \| CCL20 \| 1.399 \| DISEASES 912 \| CD1D \| 1.437 \| DISEASES 959 \| CD40LG \| 2.942 \| DISEASES 51727 \| CMPK1 \| 2.407 \| DISEASES 81035 \| COLEC12 \| 2.428 \| DISEASES 93979 \| CPA5 \| 3.978 \| DISEASES 1438 \| CSF2RA \| 1.481 \| DISEASES 1508 \| CTSB \| 1.451 \| DISEASES 8454 \| CUL1 \| 1.288 \| DISEASES 2920 \| CXCL2 \| 1.712 \| DISEASES 1621 \| DBH \| 1.047 \| DISEASES 1847 \| DUSP5 \| 1.995 \| DISEASES 10938 \| EHD1 \| 1.175 \| DISEASES 954 \| ENTPD2 \| 1.896 \| DISEASES 255324 \| EPGN \| 1.285 \| DISEASES 100302740 \| FAS-AS1 \| 2.127 \| DISEASES 54620 \| FBXL19 \| 2.801 \| DISEASES 389549 \| FEZF1 \| 1.832 \| DISEASES 2674 \| GFRA1 \| 1.421 \| DISEASES 8833 \| GMPS \| 1.692 \| DISEASES 2903 \| GRIN2A \| 1.547 \| DISEASES 3042 \| HBM \| 2.74 \| DISEASES 3098 \| HK1 \| 2.315 \| DISEASES 3320 \| HSP90AA1 \| 1.316 \| DISEASES 3384 \| ICAM2 \| 1.439 \| DISEASES 3543 \| IGLL1 \| 2.181 \| DISEASES 100423062 \| IGLL5 \| 3.525 \| DISEASES 3586 \| IL10 \| 1.719 \| DISEASES 3775 \| KCNK1 \| 2.367 \| DISEASES 10945 \| KDELR1 \| 2.335 \| DISEASES 3953 \| LEPR \| 2.617 \| DISEASES 3996 \| LLGL1 \| 1.305 \| DISEASES 5602 \| MAPK10 \| 1.357 \| DISEASES 4082 \| MARCKS \| 1.346 \| DISEASES 8972 \| MGAM \| 1.192 \| DISEASES 4583 \| MUC2 \| 2.424 \| DISEASES 4641 \| MYO1C \| 3.992 \| DISEASES 58484 \| NLRC4 \| 1.063 \| DISEASES 10577 \| NPC2 \| 1.076 \| DISEASES 100506658 \| OCLN \| 1.788 \| DISEASES 10611 \| PDLIM5 \| 1.454 \| DISEASES 5213 \| PFKM \| 1.418 \| DISEASES 5214 \| PFKP \| 1.906 \| DISEASES 5229 \| PGGT1B \| 2.155 \| DISEASES 93183 \| PIGM \| 2.591 \| DISEASES 5781 \| PTPN11 \| 2.002 \| DISEASES 5888 \| RAD51 \| 1.181 \| DISEASES 5890 \| RAD51B \| 1.603 \| DISEASES 5889 \| RAD51C \| 1.363 \| DISEASES 5892 \| RAD51D \| 1.782 \| DISEASES 5893 \| RAD52 \| 2.381 \| DISEASES 25788 \| RAD54B \| 2.373 \| DISEASES 5962 \| RDX \| 1.007 \| DISEASES 6120 \| RPE \| 2.505 \| DISEASES 6147 \| RPL23A \| 2.787 \| DISEASES 6157 \| RPL27A \| 2.805 \| DISEASES 6122 \| RPL3 \| 2.427 \| DISEASES 6204 \| RPS10 \| 2.589 \| DISEASES 51150 \| SDF4 \| 1.439 \| DISEASES 8991 \| SELENBP1 \| 1.205 \| DISEASES 200162 \| SPAG17 \| 1.784 \| DISEASES 26136 \| TES \| 1.166 \| DISEASES 9414 \| TJP2 \| 2.474 \| DISEASES 7124 \| TNF \| 1.835 \| DISEASES 8718 \| TNFRSF25 \| 1.34 \| DISEASES 94241 \| TP53INP1 \| 1.406 \| DISEASES 7177 \| TPSAB1 \| 3.414 \| DISEASES 1787 \| TRDMT1 \| 2.28 \| DISEASES 51592 \| TRIM33 \| 2.263 \| DISEASES 7247 \| TSN \| 1.771 \| DISEASES 286753 \| TUSC5 \| 1.185 \| DISEASES 7295 \| TXN \| 1.279 \| DISEASES 54600 \| UGT1A9 \| 1.518 \| DISEASES 7404 \| UTY \| 2.359 \| DISEASES 79971 \| WLS \| 1.681 \| DISEASES
Locus	(Waiting for update.)

Disease ID	1390
Disease	amebiasis
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:12) HP:0100523 \| Hepatic abscess \| 6 HP:0002583 \| Colitis \| 4 HP:0030049 \| Brain abscess \| 2 HP:0002013 \| Emesis \| 1 HP:0000822 \| Hypertension \| 1 HP:0010783 \| Erythema \| 1 HP:0002014 \| Diarrhea \| 1 HP:0005224 \| Rectal abscess \| 1 HP:0002721 \| Immunodeficiency \| 1 HP:0012219 \| Erythema nodosum \| 1 HP:0002573 \| Bloody diarrhea \| 1 HP:0000126 \| Hydronephrosis \| 1

Disease ID	1390
Disease	amebiasis
Manually Symptom	UMLS \| Name(Total Manually Symptoms:15) C1510428 \| cerebral abscesses C0701815 \| hyperchromic anemia C0267166 \| gastroduodenitis C0221014 \| secondary amyloidosis C0151594 \| bloody diarrhea C0042850 \| vitamin b complex deficiency C0038463 \| strongyloidiasis C0037285 \| skin manifestations C0037074 \| sigmoiditis C0031154 \| peritonitis C0019204 \| hepatic carcinoma C0019158 \| hepatitis C0008526 \| choroiditis C0007137 \| squamous cell carcinoma C0000727 \| acute abdomen
Text Mined Symptom	(Waiting for update.)

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

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

All Snps(Total Genotypes:1)
snpId	pubmedId	geneId	geneSymbol	diseaseId	sourceId	sentence	score	Year	geneSymbol_dbSNP	CHROMOSOME	POS	REF	ALT
rs1137101	25516614	3953	LEPR	umls:C0002438	BeFree	Humans with the Q223R leptin receptor mutation have increased susceptibility to amebiasis, but the mechanism has been unclear.	0.000542884	2015	LEPR	1	65592830	A	G

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	1390
Disease	amebiasis
Case	(Waiting for update.)

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