PedAM

Pediatric Disease Annotations & Medicines


	pars planitis

Disease ID	606
Disease	pars planitis
Definition	Form of granulomatous uveitis occurring in the region of the pars plana. This disorder is a common condition with no detectable focal pathology. It causes fibrovascular proliferation at the inferior ora serrata.
Synonym	par planitis pars planitis (disorder) pars planitis [disease/finding] planitis, pars posterior cyclitis posterior cyclitis (disorder)
OMIM	OMIM:606177
DOID	DOID:12731
UMLS	C0030593
MeSH	D015868
SNOMED-CT	SNOMEDCT_US_2016_09_01:314428001;SNOMEDCT_US_2016_09_01:45688009
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:5) C0086543 \| cataract \| 1 C0042166 \| intermediate uveitis \| 1 C0042164 \| uveitis \| 1 C0024441 \| macular hole \| 1 C0152439 \| retinoschisis \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	Entrez_id \| Symbol \| Resource(Total Genes:3) 3105 \| HLA-A \| infer 3106 \| HLA-B \| infer 3123 \| HLA-DRB1 \| infer
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:30) 2137 \| EXTL3 \| DISEASES 5949 \| RBP3 \| DISEASES 3312 \| HSPA8 \| DISEASES 1236 \| CCR7 \| DISEASES 2670 \| GFAP \| DISEASES 4069 \| LYZ \| DISEASES 898 \| CCNE1 \| DISEASES 10133 \| OPTN \| DISEASES 939 \| CD27 \| DISEASES 3001 \| GZMA \| DISEASES 1409 \| CRYAA \| DISEASES 56246 \| MRAP \| DISEASES 27087 \| B3GAT1 \| DISEASES 80381 \| CD276 \| DISEASES 3117 \| HLA-DQA1 \| DISEASES 3329 \| HSPD1 \| DISEASES 112476 \| PRRT2 \| DISEASES 3123 \| HLA-DRB1 \| DISEASES 6993 \| DYNLT1 \| DISEASES 1810 \| DR1 \| DISEASES 55315 \| SLC29A3 \| DISEASES 3127 \| HLA-DRB5 \| DISEASES 100507436 \| MICA \| DISEASES 7133 \| TNFRSF1B \| DISEASES 3105 \| HLA-A \| DISEASES 2189 \| FANCG \| DISEASES 55777 \| MBD5 \| DISEASES 6295 \| SAG \| DISEASES 3106 \| HLA-B \| DISEASES 567 \| B2M \| DISEASES
Locus	(Waiting for update.)

Disease ID	606
Disease	pars planitis
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:5) HP:0000554 \| Uveitis \| 1 HP:0030502 \| Retinoschisis \| 1 HP:0000518 \| Cataract \| 1 HP:0012124 \| Intermediate uveitis \| 1 HP:0011508 \| Macular hole \| 1

Disease ID	606
Disease	pars planitis
Manually Symptom	UMLS \| Name(Total Manually Symptoms:5) C1963229 \| retinal detachment C1417325 \| multiple sclerosis C0271051 \| macular edema C0042166 \| intermediate uveitis C0019080 \| hemorrhage
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:1) C0042166 \| intermediate uveitis \| 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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