eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| pigmented villonodular synovitis | ||||
| Disease ID | 1599 |
|---|---|
| Disease | pigmented villonodular synovitis |
| Definition | Diffuse outgrowth arising from the SYNOVIAL MEMBRANE; SYNOVIAL BURSA; or TENDON sheath around the joint cavity, with extension to surrounding soft tissue. It is characterized by pigmented HEMOSIDERIN-containing MACROPHAGES; FOAM CELLS; and multinucleated GIANT CELLS. It usually occurs in the hands and feet, and around large joints, such as in the ankle and knee joints. |
| Synonym | chronic haemorrhagic villous synovitis chronic hemorrhagic villous synovitis diffuse giant cell neoplasm of tendon sheath diffuse giant cell neoplasm of tenosynovium diffuse giant cell neoplasm of the tenosynovium diffuse giant cell tumor of tendon sheath diffuse giant cell tumor of tenosynovium diffuse giant cell tumor of the tenosynovium diffuse tenosynovial giant cell neoplasm diffuse tenosynovial giant cell tumor pigmented synovitis villonodular pigmented villonodular synovitides pigmented villonodular synovitis (disorder) pvns - pigmented villonodular synovitis synovitides, pigmented villonodular synovitis, pigmented villonodular synovitis, pigmented villonodular [disease/finding] synovitis, villonodular, pigmented tenosynovial giant cell tumor, diffuse tenosynovial giant cell tumor, diffuse (morphologic abnormality) tenosynovial giant cell tumor, diffuse type tenosynovial giant cell tumour, diffuse villonodular synovitides, pigmented villonodular synovitis villonodular synovitis, pigmented villous tenosynovitis |
| Orphanet | |
| DOID | |
| UMLS | C0039106 |
| MeSH | |
| SNOMED-CT | |
| 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:28) 241 | ALOX5AP | 1.728 | DISEASES 23141 | ANKLE2 | 3.621 | DISEASES 799 | CALCR | 2.626 | DISEASES 800 | CALD1 | 1.395 | DISEASES 9332 | CD163 | 2.573 | DISEASES 1378 | CR1 | 1.645 | DISEASES 1380 | CR2 | 1.024 | DISEASES 1435 | CSF1 | 4.804 | DISEASES 1791 | DNTT | 1.294 | DISEASES 2153 | F5 | 1.653 | DISEASES 9446 | GSTO1 | 1.734 | DISEASES 3652 | IPP | 2.107 | DISEASES 27030 | MLH3 | 2.354 | DISEASES 4318 | MMP9 | 1.917 | DISEASES 4318 | MMP9 | 1.503 | DISEASES 4763 | NF1 | 1.158 | DISEASES 126014 | OSCAR | 2.122 | DISEASES 56666 | PANX2 | 2.968 | DISEASES 6490 | PMEL | 1.173 | DISEASES 5788 | PTPRC | 1.082 | DISEASES 5817 | PVR | 3.412 | DISEASES 5817 | PVR | 1.572 | DISEASES 6452 | SH3BP2 | 2.383 | DISEASES 23583 | SMUG1 | 1.994 | DISEASES 26783 | SNORA65 | 4.113 | DISEASES 6654 | SOS1 | 2.535 | DISEASES 7133 | TNFRSF1B | 1.54 | DISEASES 7316 | UBC | 1.721 | DISEASES |
| Locus | (Waiting for update.) |
| Disease ID | 1599 |
|---|---|
| Disease | pigmented villonodular synovitis |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:2) |
| Disease ID | 1599 |
|---|---|
| Disease | pigmented villonodular synovitis |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:3) |
| Text Mined Symptom | (Waiting for update.) |
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 | 1599 |
|---|---|
| Disease | pigmented villonodular synovitis |
| Case | (Waiting for update.) |