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PedAM

Pediatric Disease Annotations & Medicines



   chondroma
  

Disease ID 927
Disease chondroma
Definition
A benign neoplasm derived from mesodermal cells that form cartilage. It may remain within the substance of a cartilage or bone (true chondroma or enchondroma) or may develop on the surface of a cartilage (ecchondroma or ecchondrosis). (Dorland, 27th ed; Stedman, 25th ed)
Synonym
[m]chondroma nos
[m]chondroma nos (morphologic abnormality)
chondroma (morphologic abnormality)
chondroma [disease/finding]
chondroma, benign
chondroma, nos
chondromas
DOID
UMLS
C0936248
MeSH
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:5)
C0008441  |  chondroblastoma  |  1
C0238198  |  gastrointestinal stromal tumor  |  1
C0020492  |  hyperostosis  |  1
C0008925  |  cleft palate  |  1
C0879615  |  stromal tumor  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:2)
IDH2  |  3418  |  CTD_human
IDH1  |  3417  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:56)
6790  |  AURKA  |  DISEASES
3312  |  HSPA8  |  DISEASES
55907  |  CMAS  |  DISEASES
5947  |  RBP1  |  DISEASES
3554  |  IL1R1  |  DISEASES
4035  |  LRP1  |  DISEASES
6659  |  SOX4  |  DISEASES
25796  |  PGLS  |  DISEASES
2521  |  FUS  |  DISEASES
5156  |  PDGFRA  |  DISEASES
6302  |  TSPAN31  |  DISEASES
3417  |  IDH1  |  DISEASES
57534  |  MIB1  |  DISEASES
6521  |  SLC4A1  |  DISEASES
9739  |  SETD1A  |  DISEASES
6389  |  SDHA  |  DISEASES
7157  |  TP53  |  DISEASES
2212  |  FCGR2A  |  DISEASES
1030  |  CDKN2B  |  DISEASES
7070  |  THY1  |  DISEASES
3815  |  KIT  |  DISEASES
6781  |  STC1  |  DISEASES
2215  |  FCGR3B  |  DISEASES
3549  |  IHH  |  DISEASES
27087  |  B3GAT1  |  DISEASES
947  |  CD34  |  DISEASES
1604  |  CD55  |  DISEASES
4026  |  LPP  |  DISEASES
5745  |  PTH1R  |  DISEASES
1879  |  EBF1  |  DISEASES
51341  |  ZBTB7A  |  DISEASES
3052  |  HCCS  |  DISEASES
3418  |  IDH2  |  DISEASES
2246  |  FGF1  |  DISEASES
5348  |  FXYD1  |  DISEASES
55107  |  ANO1  |  DISEASES
2213  |  FCGR2B  |  DISEASES
7042  |  TGFB2  |  DISEASES
2214  |  FCGR3A  |  DISEASES
6391  |  SDHC  |  DISEASES
2209  |  FCGR1A  |  DISEASES
6441  |  SFTPD  |  DISEASES
6390  |  SDHB  |  DISEASES
6392  |  SDHD  |  DISEASES
3303  |  HSPA1A  |  DISEASES
2131  |  EXT1  |  DISEASES
10186  |  LHFP  |  DISEASES
4507  |  MTAP  |  DISEASES
4781  |  NFIB  |  DISEASES
2591  |  GALNT3  |  DISEASES
8091  |  HMGA2  |  DISEASES
3778  |  KCNMA1  |  DISEASES
4193  |  MDM2  |  DISEASES
1649  |  DDIT3  |  DISEASES
84525  |  HOPX  |  DISEASES
3316  |  HSPB2  |  DISEASES
Locus(Waiting for update.)
Disease ID 927
Disease chondroma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:7)
HP:0100723  |  Gastrointestinal stroma tumor  |  2
HP:0002664  |  Neoplasia  |  1
HP:0030432  |  Chondroblastoma  |  1
HP:0040184  |  Oral hemorrhage  |  1
HP:0100246  |  Osteoma  |  1
HP:0100774  |  Hyperostosis  |  1
HP:0000175  |  Palatoschisis  |  1
Disease ID 927
Disease chondroma
Manually Symptom
UMLS  | Name(Total Manually Symptoms:1)
C1608408  |  malignant transformation
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
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.)