PedAM

Pediatric Disease Annotations & Medicines


	erythema infectiosum

Disease ID	1490
Disease	erythema infectiosum
Definition	Contagious infection with human B19 Parvovirus most commonly seen in school age children and characterized by fever, headache, and rashes of the face, trunk, and extremities. It is often confused with rubella.
Synonym	erythema contagiosum erythema infectiosum (disorder) erythema infectiosum (fifth disease) erythema infectiosum [disease/finding] fifth dis fifth disease parvovirus b19 infection slap cheek syndrome slapped cheek syndrome
DOID	DOID:8743
UMLS	C0085273
MeSH	D016731
SNOMED-CT	SNOMEDCT_US_2016_09_01:34730008
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:41) C0002871 \| anemia \| 7 C0281963 \| red cell aplasia \| 4 C0019158 \| hepatitis \| 3 C0027121 \| myositis \| 3 C0017658 \| glomerulonephritis \| 3 C0002871 \| anaemia \| 3 C0026975 \| myelitis \| 2 C0015530 \| factor xiii deficiency \| 2 C0031046 \| pericarditis \| 2 C0034902 \| pure red cell aplasia \| 2 C0002874 \| aplastic anemia \| 2 C0235025 \| motor neuropathy \| 1 C0020305 \| hydrops fetalis \| 1 C0549423 \| obstructive hydrocephalus \| 1 C0699743 \| congenital muscular dystrophy \| 1 C0014038 \| encephalitis \| 1 C0024141 \| systemic lupus erythematosus \| 1 C0020305 \| hydrops foetalis \| 1 C0026850 \| muscular dystrophy \| 1 C0085669 \| acute leukemia \| 1 C0018378 \| guillain-barre syndrome \| 1 C0009447 \| common variable immunodeficiency \| 1 C0030312 \| bone marrow failure \| 1 C0002878 \| hemolytic anemia \| 1 C0040147 \| thyroiditis \| 1 C0024291 \| hemophagocytic syndrome \| 1 C0494491 \| mononeuropathy \| 1 C0000786 \| spontaneous abortion \| 1 C0024291 \| hemophagocytic lymphohistiocytosis \| 1 C0442874 \| neuropathy \| 1 C0032231 \| pleuritis \| 1 C0002880 \| autoimmune hemolytic anemia \| 1 C0409974 \| lupus erythematosus \| 1 C0011847 \| diabetes \| 1 C0677607 \| hashimoto's thyroiditis \| 1 C0011849 \| diabetes mellitus \| 1 C0455988 \| non-immune hydrops fetalis \| 1 C0011854 \| type 1 diabetes \| 1 C0037889 \| hereditary spherocytosis \| 1 C0020255 \| hydrocephalus \| 1 C0011854 \| type 1 diabetes mellitus \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	Entrez_id \| Symbol \| Resource(Total Genes:5) 3458 \| IFNG \| infer 3586 \| IL10 \| infer 3569 \| IL6 \| infer 7040 \| TGFB1 \| infer 7124 \| TNF \| infer
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:33) 350 \| APOH \| DISEASES 5816 \| PVALB \| DISEASES 2218 \| FKTN \| DISEASES 5657 \| PRTN3 \| DISEASES 5300 \| PIN1 \| DISEASES 79733 \| E2F8 \| DISEASES 4924 \| NUCB1 \| DISEASES 8365 \| HIST1H4H \| DISEASES 51151 \| SLC45A2 \| DISEASES 8360 \| HIST1H4D \| DISEASES 8294 \| HIST1H4I \| DISEASES 8363 \| HIST1H4J \| DISEASES 8368 \| HIST1H4L \| DISEASES 8362 \| HIST1H4K \| DISEASES 5169 \| ENPP3 \| DISEASES 121504 \| HIST4H4 \| DISEASES 8359 \| HIST1H4A \| DISEASES 8367 \| HIST1H4E \| DISEASES 554313 \| HIST2H4B \| DISEASES 8370 \| HIST2H4A \| DISEASES 959 \| CD40LG \| DISEASES 5476 \| CTSA \| DISEASES 2623 \| GATA1 \| DISEASES 8366 \| HIST1H4B \| DISEASES 8361 \| HIST1H4F \| DISEASES 8364 \| HIST1H4C \| DISEASES 3980 \| LIG3 \| DISEASES 1874 \| E2F4 \| DISEASES 1876 \| E2F6 \| DISEASES 1365 \| CLDN3 \| DISEASES 1875 \| E2F5 \| DISEASES 246734 \| NPCDR1 \| DISEASES 100128252 \| ZNF667-AS1 \| DISEASES
Locus	(Waiting for update.)

Disease ID	1490
Disease	erythema infectiosum
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:44) HP:0001903 \| Anemia \| 9 HP:0000969 \| Dropsy \| 4 HP:0012410 \| Pure red cell aplasia \| 4 HP:0012115 \| Liver inflammation \| 3 HP:0000099 \| Glomerular nephritis \| 3 HP:0100614 \| Muscle inflammation \| 3 HP:0001915 \| Aplastic anemia \| 2 HP:0001298 \| Encephalopathy \| 2 HP:0001701 \| Pericarditis \| 2 HP:0012486 \| Inflammation of spinal cord \| 2 HP:0002102 \| Pleuritis \| 1 HP:0009831 \| Single damaged nerve \| 1 HP:0002072 \| Chorea \| 1 HP:0012133 \| Erythroid hypoplasia \| 1 HP:0000597 \| Ophthalmoparesis \| 1 HP:0001541 \| Ascites \| 1 HP:0003560 \| Muscular dystrophy \| 1 HP:0002720 \| Decreased immunoglobulin A \| 1 HP:0100646 \| Thyroiditis \| 1 HP:0002383 \| Encephalitis \| 1 HP:0002126 \| Polymicrogyria \| 1 HP:0000238 \| Nonsyndromal hydrocephalus \| 1 HP:0002725 \| Systemic lupus erythematosus \| 1 HP:0005528 \| Bone marrow hypoplasia \| 1 HP:0005268 \| Spontaneous abortion \| 1 HP:0002901 \| Hypocalcemia \| 1 HP:0000819 \| Diabetes mellitus \| 1 HP:0004444 \| Spherocytosis \| 1 HP:0010783 \| Erythema \| 1 HP:0005510 \| Transient decrease in blood erythrocyte number \| 1 HP:0002488 \| Acute leukemias \| 1 HP:0200119 \| Acute liver inflammation \| 1 HP:0001399 \| Liver failure \| 1 HP:0003741 \| Muscular dystrophy, congenital \| 1 HP:0001791 \| Fetal ascites \| 1 HP:0001890 \| Autoimmune hemolytic anemia \| 1 HP:0001878 \| Haemolytic anaemia \| 1 HP:0001789 \| Hydrops fetalis \| 1 HP:0007430 \| Generalized edema \| 1 HP:0004448 \| Fulminant hepatic failure \| 1 HP:0000872 \| Hashimoto's thyroiditis \| 1 HP:0003201 \| Rhabdomyolysis \| 1 HP:0002721 \| Immunodeficiency \| 1 HP:0200123 \| Chronic liver inflammation \| 1

Disease ID	1490
Disease	erythema infectiosum
Manually Symptom	(Waiting for update.)
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:14) C0002871 \| anemia \| 6 C0281963 \| red cell aplasia \| 4 C1096155 \| macrophage activation syndrome \| 2 C0037285 \| skin manifestation \| 2 C0002874 \| aplastic anemia \| 2 C0034902 \| pure red cell aplasia \| 2 C0162538 \| iga deficiency \| 1 C0877221 \| erythroblastopenia \| 1 C0409974 \| lupus erythematosus \| 1 C0031256 \| petechial rash \| 1 C0751341 \| infectious myelitis \| 1 C0020305 \| hydrops fetalis \| 1 C0455988 \| non-immune hydrops fetalis \| 1 C0024141 \| systemic lupus erythematosus \| 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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