PedAM
Pediatric Disease Annotations & Medicines
| ependymoblastoma | ||||
| Disease ID | 1427 |
|---|---|
| Disease | ependymoblastoma |
| Definition | A highly malignant embryonal tumor of infancy and young childhood characterized by neuroectodermal elements organized in distinctive multilayered rosettes. Ependymoblastomas are large lesions that occur in the supratentorial compartment, typically displaying a physical connection to the ventricular system. [] |
| Synonym | ependymoblastoma (disorder) ependymoblastoma (morphologic abnormality) ependymoblastomas |
| Orphanet | |
| DOID | |
| UMLS | C0700367 |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:2) |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:37) 7431 | VIM | DISEASES 3558 | IL2 | DISEASES 3458 | IFNG | DISEASES 2026 | ENO2 | DISEASES 2023 | ENO1 | DISEASES 27189 | IL17C | DISEASES 6351 | CCL4 | DISEASES 5894 | RAF1 | DISEASES 2670 | GFAP | DISEASES 2521 | FUS | DISEASES 79727 | LIN28A | DISEASES 759 | CA1 | DISEASES 4659 | PPP1R12A | DISEASES 6598 | SMARCB1 | DISEASES 6855 | SYP | DISEASES 7157 | TP53 | DISEASES 4613 | MYCN | DISEASES 7070 | THY1 | DISEASES 27165 | GLS2 | DISEASES 2744 | GLS | DISEASES 4684 | NCAM1 | DISEASES 1789 | DNMT3B | DISEASES 10215 | OLIG2 | DISEASES 389421 | LIN28B | DISEASES 1499 | CTNNB1 | DISEASES 126014 | OSCAR | DISEASES 4133 | MAP2 | DISEASES 10763 | NES | DISEASES 8349 | HIST2H2BE | DISEASES 4803 | NGF | DISEASES 642489 | FKBP1C | DISEASES 6342 | SCP2 | DISEASES 5476 | CTSA | DISEASES 4609 | MYC | DISEASES 2280 | FKBP1A | DISEASES 4599 | MX1 | DISEASES 4914 | NTRK1 | DISEASES |
| Locus | (Waiting for update.) |
| Disease ID | 1427 |
|---|---|
| Disease | ependymoblastoma |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:3) HP:0030065 | Primitive neuroectodermal tumor | 1 HP:0002888 | Ependymoma | 1 HP:0001289 | Confusion | 1 |
| Disease ID | 1427 |
|---|---|
| Disease | ependymoblastoma |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:1) C1704231 | meningeal metastases |
| Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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| (Waiting for update.) |
All Snps(Total Genotypes:0) | |
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| (Waiting for update.) | |
GWASdb Annotation(Total Genotypes:0) | |
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| (Waiting for update.) | |
GWASdb Snp Trait(Total Genotypes:0) | |
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| (Waiting for update.) | |
Mapped by lexical matching(Total Items:0) |
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| (Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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| (Waiting for update.) |
Chemical(Total Drugs:0) | |
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| (Waiting for update.) | |
FDA approved drug and dosage information(Total Drugs:0) | |
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| (Waiting for update.) | |
FDA labeling changes(Total Drugs:0) | |
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| (Waiting for update.) | |