eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| solitary fibrous tumor | ||||
| Disease ID | 1517 |
|---|---|
| Disease | solitary fibrous tumor |
| Definition | Rare neoplasms of mesenchymal origin, usually benign, and most commonly involving the PLEURA (see SOLITARY FIBROUS TUMOR, PLEURAL). They also are found in extrapleural sites. |
| Synonym | fibrous tumor, solitary fibrous tumors, solitary localised fibrous tumour localized fibrous tumor sft solitary fibrous tumor (morphologic abnormality) solitary fibrous tumors solitary fibrous tumors [disease/finding] solitary fibrous tumour tumor, solitary fibrous tumors, solitary fibrous |
| Orphanet | |
| UMLS | C1266119 |
| MeSH | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:18) C0020598 | hypoglycemia | 3 C0004114 | astrocytoma | 1 C0002871 | anemia | 1 C0023827 | liposarcomas | 1 C0002880 | autoimmune hemolytic anemia | 1 C0002878 | hemolytic anemia | 1 C1145670 | respiratory failure | 1 C0242379 | lung cancer | 1 C0238463 | papillary thyroid carcinoma | 1 C0007115 | thyroid ca | 1 C0020437 | hypercalcemia | 1 C0220650 | brain metastases | 1 C0879615 | stromal tumor | 1 C0018552 | hamartoma | 1 C0334583 | pilocytic astrocytoma | 1 C0549473 | thyroid carcinoma | 1 C0149925 | small cell lung cancer | 1 C0018922 | haemangiopericytoma | 1 |
| Curated Gene | Entrez_id | Symbol | Resource(Total Genes:2) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | (Waiting for update.) |
| Locus | Symbol | Locus(Total Locus:2) |
| Disease ID | 1517 |
|---|---|
| Disease | solitary fibrous tumor |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:18) HP:0002664 | Neoplasia | 4 HP:0001943 | Hypoglycemia | 3 HP:0012151 | Hemothorax | 1 HP:0100029 | Lingual thyroid | 1 HP:0009592 | Astrocytoma | 1 HP:0002878 | Respiratory failure | 1 HP:0002890 | Thyroid carcinoma | 1 HP:0030731 | Carcinoma | 1 HP:0001878 | Haemolytic anaemia | 1 HP:0010566 | Hamartoma | 1 HP:0001548 | Overgrowth | 1 HP:0001903 | Anemia | 1 HP:0001978 | Extramedullary hematopoiesis | 1 HP:0030357 | Small cell lung carcinoma | 1 HP:0002895 | Papillary thyroid carcinoma | 1 HP:0001890 | Autoimmune hemolytic anemia | 1 HP:0003072 | Hypercalcemia | 1 HP:0002835 | Aspiration | 1 |
| Disease ID | 1517 |
|---|---|
| Disease | solitary fibrous tumor |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:4) |
| Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:1) |
Manually Genotype(Total Text Mining Genotypes:0) |
|---|
| (Waiting for update.) |
Text Mining Genotype(Total 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) |
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| (Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
|---|
| (Waiting for update.) |
| Disease ID | 1517 |
|---|---|
| Disease | solitary fibrous tumor |
| Case | (Waiting for update.) |