PedAM

Pediatric Disease Annotations & Medicines


	ocular toxoplasmosis

Disease ID	984
Disease	ocular toxoplasmosis
Definition	Infection caused by the protozoan parasite TOXOPLASMA in which there is extensive connective tissue proliferation, the retina surrounding the lesions remains normal, and the ocular media remain clear. Chorioretinitis may be associated with all forms of toxoplasmosis, but is usually a late sequel of congenital toxoplasmosis. The severe ocular lesions in infants may lead to blindness.
Synonym	ocular toxoplasmoses ocular toxoplasmosis (disorder) toxoplasmoses, ocular toxoplasmosis, ocular toxoplasmosis, ocular [disease/finding]
DOID	DOID:13343
UMLS	C0040561
MeSH	D014126
SNOMED-CT	SNOMEDCT_US_2016_09_01:416481006
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:12) C0042164 \| uveitis \| 4 C0042167 \| posterior uveitis \| 2 C0035305 \| retinal detachment \| 1 C0035335 \| retinoblastoma \| 1 C0039128 \| syphilis \| 1 C0008513 \| retinochoroiditis \| 1 C0040560 \| congenital toxoplasmosis \| 1 C0456909 \| vision loss \| 1 C0162293 \| papillitis \| 1 C0042384 \| angiitis \| 1 C0035302 \| retinal artery occlusion \| 1 C0040558 \| toxoplasmosis \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) 3458 \| IFNG \| infer
Text Mined Gene	(Waiting for update.)
Locus	(Waiting for update.)

Disease ID	984
Disease	ocular toxoplasmosis
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:11) HP:0000554 \| Uveitis \| 4 HP:0012123 \| Posterior uveitis \| 2 HP:0000572 \| Visual loss \| 1 HP:0001141 \| Severe visual impairment \| 1 HP:0007868 \| ARMD \| 1 HP:0011531 \| Hyalitis \| 1 HP:0002633 \| Vasculitis \| 1 HP:0009919 \| Retinoblastoma \| 1 HP:0000505 \| Poor vision \| 1 HP:0000541 \| Detached retina \| 1 HP:0007777 \| Chorioretinal scar \| 1

Disease ID	984
Disease	ocular toxoplasmosis
Manually Symptom	UMLS \| Name(Total Manually Symptoms:10) C1963229 \| retinal detachment C0796095 \| c syndrome C0456909 \| blindness C0162293 \| papillitis C0152026 \| retinal vasculitis C0042164 \| intraocular inflammation C0040558 \| toxoplasma gondii infections C0035334 \| pigmentary retinopathy C0035333 \| retinitis C0029896 \| ent disease
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:2) C0162293 \| papillitis \| 1 C0035305 \| retinal detachment \| 1

Manually Genotype(Total Text Mining Genotypes:0)
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All Snps(Total Genotypes:0)
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GWASdb Annotation(Total Genotypes:0)
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GWASdb Snp Trait(Total Genotypes:0)
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Mapped by lexical matching(Total Items:0)
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Mapped by homologous gene(Total Items:0)
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Chemical(Total Drugs:0)
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FDA approved drug and dosage information(Total Drugs:0)
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FDA labeling changes(Total Drugs:0)
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