PedAM
Pediatric Disease Annotations & Medicines
| chordoid glioma | ||||
| Disease ID | 1719 |
|---|---|
| Disease | chordoid glioma |
| Definition | A rare, slow-growing neuroepithelial neoplasm of uncertain origin affecting adults. It is located in the third ventricle. It is characterized by the presence of epithelioid cells which express GFAP, and mucinous stroma which contains lymphoplasmacytic infiltrates. |
| Synonym | chordoid glioma (disorder) chordoid glioma (morphologic abnormality) chordoid glioma of 3rd ventricle chordoid glioma of the 3rd ventricle chordoid glioma of the third ventricle chordoid glioma of the third ventricle (who grade ii) chordoid glioma of third ventricle third ventricle chordoid glioma |
| Orphanet | |
| DOID | |
| UMLS | C1322252 |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:1) |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:30) 2026 | ENO2 | DISEASES 6659 | SOX4 | DISEASES 7166 | TPH1 | DISEASES 15 | AANAT | DISEASES 2670 | GFAP | DISEASES 3417 | IDH1 | DISEASES 6598 | SMARCB1 | DISEASES 4072 | EPCAM | DISEASES 7157 | TP53 | DISEASES 6581 | SLC22A3 | DISEASES 1956 | EGFR | DISEASES 5458 | POU4F2 | DISEASES 7015 | TERT | DISEASES 947 | CD34 | DISEASES 3418 | IDH2 | DISEASES 4771 | NF2 | DISEASES 7080 | NKX2-1 | DISEASES 5802 | PTPRS | DISEASES 6004 | RGS16 | DISEASES 51684 | SUFU | DISEASES 1301 | COL11A1 | DISEASES 94233 | OPN4 | DISEASES 6194 | RPS6 | DISEASES 438 | ASMT | DISEASES 5991 | RFX3 | DISEASES 3875 | KRT18 | DISEASES 3239 | HOXD13 | DISEASES 1365 | CLDN3 | DISEASES 23532 | PRAME | DISEASES 79776 | ZFHX4 | DISEASES |
| Locus | (Waiting for update.) |
| Disease ID | 1719 |
|---|---|
| Disease | chordoid glioma |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:2) |
| Disease ID | 1719 |
|---|---|
| Disease | chordoid glioma |
| Manually Symptom | (Waiting for update.) |
| 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.) | |