myxopapillary ependymoma |
Disease ID | 1425 |
---|---|
Disease | myxopapillary ependymoma |
Definition | A slow growing, WHO grade I glioma which generally occurs in young adults. It arises almost exclusively in the conus medullaris, cauda equina, and filum terminale of the spinal cord. It generally has a favorable prognosis and is characterized histologically by tumor cells arranged in a papillary manner around vascularized mucoid stromal cores. (Adapted from WHO). |
Synonym | ependymoma, benign ependymoma, myxopapillary ependymomas, myxopapillary myxopapillary ependymoma (morphologic abnormality) myxopapillary ependymomas |
Orphanet | |
DOID | |
UMLS | C0205769 |
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:36) 55644 | OSGEP | DISEASES 1048 | CEACAM5 | DISEASES 2026 | ENO2 | DISEASES 3852 | KRT5 | DISEASES 2670 | GFAP | DISEASES 3958 | LGALS3 | DISEASES 10752 | CHL1 | DISEASES 999 | CDH1 | DISEASES 5159 | PDGFRB | DISEASES 6855 | SYP | DISEASES 7157 | TP53 | DISEASES 26040 | SETBP1 | DISEASES 760 | CA2 | DISEASES 909 | CD1A | DISEASES 10481 | HOXB13 | DISEASES 3856 | KRT8 | DISEASES 9965 | FGF19 | DISEASES 4323 | MMP14 | DISEASES 3090 | HIC1 | DISEASES 5315 | PKM | DISEASES 3052 | HCCS | DISEASES 3855 | KRT7 | DISEASES 9146 | HGS | DISEASES 4221 | MEN1 | DISEASES 23136 | EPB41L3 | DISEASES 4771 | NF2 | DISEASES 2035 | EPB41 | DISEASES 11186 | RASSF1 | DISEASES 2673 | GFPT1 | DISEASES 2736 | GLI2 | DISEASES 51684 | SUFU | DISEASES 2315 | MLANA | DISEASES 174 | AFP | DISEASES 146713 | RBFOX3 | DISEASES 9212 | AURKB | DISEASES 79104 | MEG8 | DISEASES |
Locus | (Waiting for update.) |
Disease ID | 1425 |
---|---|
Disease | myxopapillary ependymoma |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:4) HP:0003418 | Back pain | 2 HP:0012531 | Pain | 1 HP:0040184 | Oral hemorrhage | 1 HP:0002664 | Neoplasia | 1 |
Disease ID | 1425 |
---|---|
Disease | myxopapillary ependymoma |
Manually Symptom | UMLS | Name(Total Manually Symptoms:2) |
Text Mined Symptom | (Waiting for update.) |
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.) |