PedAM

Pediatric Disease Annotations & Medicines


	strongyloidiasis

Disease ID	756
Disease	strongyloidiasis
Definition	Infection with nematodes of the genus STRONGYLOIDES. The presence of larvae may produce pneumonitis and the presence of adult worms in the intestine could lead to moderate to severe diarrhea.
Synonym	[x]strongyloidiasis, unspecified [x]strongyloidiasis, unspecified (disorder) infection by strongyloides infection by strongyloides (disorder) infection by strongyloides, nos infection caused by strongyloides infection caused by strongyloides (disorder) strongylodiasis strongyloides infection strongyloidiases strongyloidiasis [disease/finding] strongyloidosis
Orphanet	ORPHANET:76
DOID	DOID:10955
UMLS	C0038463
MeSH	D013322
SNOMED-CT	SNOMEDCT_US_2016_09_01:1214006
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:16) C0025289 \| meningitis \| 3 C0017662 \| membranoproliferative glomerulonephritis \| 2 C0017658 \| glomerulonephritis \| 2 C0085437 \| bacterial meningitis \| 2 C0235618 \| proliferative glomerulonephritis \| 2 C0178238 \| intestinal infections \| 1 C0409974 \| lupus erythematosus \| 1 C1522378 \| large granular lymphocytosis \| 1 C0002871 \| anemia \| 1 C0035435 \| rheumatic disease \| 1 C0024141 \| systemic lupus erythematosus \| 1 C0036323 \| schistosomiasis \| 1 C0017536 \| giardiasis \| 1 C0178238 \| intestinal infection \| 1 C0035435 \| rheumatic diseases \| 1 C0042769 \| virus infection \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:52) 4282 \| MIF \| DISEASES 973 \| CD79A \| DISEASES 3565 \| IL4 \| DISEASES 3567 \| IL5 \| DISEASES 5266 \| PI3 \| DISEASES 3417 \| IDH1 \| DISEASES 3959 \| LGALS3BP \| DISEASES 2208 \| FCER2 \| DISEASES 5443 \| POMC \| DISEASES 409 \| ARRB2 \| DISEASES 963 \| CD53 \| DISEASES 2212 \| FCGR2A \| DISEASES 83447 \| SLC25A31 \| DISEASES 7547 \| ZIC3 \| DISEASES 4681 \| NBL1 \| DISEASES 213 \| ALB \| DISEASES 6356 \| CCL11 \| DISEASES 116984 \| ARAP2 \| DISEASES 171558 \| PTCRA \| DISEASES 9451 \| EIF2AK3 \| DISEASES 126669 \| SHE \| DISEASES 79834 \| PEAK1 \| DISEASES 4843 \| NOS2 \| DISEASES 255324 \| EPGN \| DISEASES 3418 \| IDH2 \| DISEASES 4521 \| NUDT1 \| DISEASES 3329 \| HSPD1 \| DISEASES 29949 \| IL19 \| DISEASES 9623 \| TCL1B \| DISEASES 80781 \| COL18A1 \| DISEASES 404552 \| SCGB1D4 \| DISEASES 2213 \| FCGR2B \| DISEASES 56980 \| PRDM10 \| DISEASES 4512 \| MT-CO1 \| DISEASES 84946 \| LTV1 \| DISEASES 4942 \| OAT \| DISEASES 959 \| CD40LG \| DISEASES 2623 \| GATA1 \| DISEASES 6518 \| SLC2A5 \| DISEASES 127262 \| TPRG1L \| DISEASES 833 \| CARS \| DISEASES 90865 \| IL33 \| DISEASES 2235 \| FECH \| DISEASES 7932 \| OR2H2 \| DISEASES 7110 \| TMF1 \| DISEASES 279 \| AMY2A \| DISEASES 408 \| ARRB1 \| DISEASES 3712 \| IVD \| DISEASES 503542 \| SPRN \| DISEASES 246744 \| STH \| DISEASES 56342 \| PPAN \| DISEASES 11201 \| POLI \| DISEASES
Locus	(Waiting for update.)

Disease ID	756
Disease	strongyloidiasis
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:11) HP:0001880 \| Eosinophilia \| 4 HP:0001287 \| Meningitis \| 2 HP:0000793 \| Membranoproliferative glomerulonephritis \| 2 HP:0000099 \| Glomerular nephritis \| 2 HP:0003146 \| Decreased circulating cholesterol level \| 1 HP:0002716 \| Lymph node hyperplasia \| 1 HP:0002239 \| Gastrointestinal hemorrhage \| 1 HP:0001903 \| Anemia \| 1 HP:0001945 \| Fever \| 1 HP:0002584 \| Intestinal hemorrhage \| 1 HP:0002725 \| Systemic lupus erythematosus \| 1

Disease ID	756
Disease	strongyloidiasis
Manually Symptom	UMLS \| Name(Total Manually Symptoms:28) C2240374 \| eosinophilia C1963165 \| malabsorption C1963084 \| colitis C1839611 \| n syndrome C1704321 \| minimal change nephrotic syndrome C1522057 \| duodenitis C1384353 \| parasitic infestation C1257845 \| pseudomembranous enteritis C1090821 \| sepsis C0853793 \| enterococcal meningitis C0277792 \| pathognomonic sign C0267375 \| chronic colitis C0264490 \| acute respiratory failure C0263338 \| chronic urticaria C0239182 \| watery diarrhea C0033680 \| protein-losing enteropathy C0030446 \| paralytic ileus C0027726 \| nephrotic syndrome C0024291 \| hemophagocytic syndrome C0023501 \| leukemoid reaction C0023048 \| larva migrans C0021843 \| intestinal obstruction C0021831 \| enteropathy C0021141 \| syndrome of inappropriate secretion of antidiuretic hormone C0020097 \| htlv-i infection C0015230 \| rash C0011991 \| diarrhoea C0004623 \| bacterial infections
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:3) C0014457 \| eosinophilia \| 4 C1839611 \| n syndrome \| 2 C0027721 \| minimal change nephrotic syndrome \| 1

Manually Genotype(Total Text Mining 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.)

Chemical(Total Drugs:0)
(Waiting for update.)

FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)

FDA labeling changes(Total Drugs:0)
(Waiting for update.)

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