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PedAM

Pediatric Disease Annotations & Medicines



   pigmented villonodular synovitis
  

Disease ID 951
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)
C0003873  |  rheumatoid arthritis  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:55)
113278  |  SLC52A3  |  DISEASES
54  |  ACP5  |  DISEASES
3312  |  HSPA8  |  DISEASES
2026  |  ENO2  |  DISEASES
55856  |  ACOT13  |  DISEASES
8600  |  TNFSF11  |  DISEASES
4656  |  MYOG  |  DISEASES
4654  |  MYOD1  |  DISEASES
968  |  CD68  |  DISEASES
1116  |  CHI3L1  |  DISEASES
3685  |  ITGAV  |  DISEASES
6598  |  SMARCB1  |  DISEASES
9410  |  SNRNP40  |  DISEASES
4123  |  MAN2C1  |  DISEASES
7157  |  TP53  |  DISEASES
963  |  CD53  |  DISEASES
275  |  AMT  |  DISEASES
526  |  ATP6V1B2  |  DISEASES
4851  |  NOTCH1  |  DISEASES
1436  |  CSF1R  |  DISEASES
7805  |  LAPTM5  |  DISEASES
1293  |  COL6A3  |  DISEASES
4286  |  MITF  |  DISEASES
64112  |  MOAP1  |  DISEASES
9317  |  PTER  |  DISEASES
947  |  CD34  |  DISEASES
1604  |  CD55  |  DISEASES
1435  |  CSF1  |  DISEASES
23583  |  SMUG1  |  DISEASES
7316  |  UBC  |  DISEASES
27030  |  MLH3  |  DISEASES
23141  |  ANKLE2  |  DISEASES
4763  |  NF1  |  DISEASES
9332  |  CD163  |  DISEASES
799  |  CALCR  |  DISEASES
126014  |  OSCAR  |  DISEASES
800  |  CALD1  |  DISEASES
1378  |  CR1  |  DISEASES
1380  |  CR2  |  DISEASES
5788  |  PTPRC  |  DISEASES
2153  |  F5  |  DISEASES
9446  |  GSTO1  |  DISEASES
1791  |  DNTT  |  DISEASES
4318  |  MMP9  |  DISEASES
4318  |  MMP9  |  DISEASES
7133  |  TNFRSF1B  |  DISEASES
241  |  ALOX5AP  |  DISEASES
56666  |  PANX2  |  DISEASES
3652  |  IPP  |  DISEASES
6654  |  SOS1  |  DISEASES
5817  |  PVR  |  DISEASES
5817  |  PVR  |  DISEASES
6490  |  PMEL  |  DISEASES
6452  |  SH3BP2  |  DISEASES
26783  |  SNORA65  |  DISEASES
Locus(Waiting for update.)
Disease ID 951
Disease pigmented villonodular synovitis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:2)
HP:0001289  |  Confusion  |  1
HP:0001370  |  Rheumatoid arthritis  |  1
Disease ID 951
Disease pigmented villonodular synovitis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:3)
C0154743  |  ulnar neuropathy
C0085077  |  sweet's syndrome
C0018924  |  hemarthrosis
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.)