PedAM

Pediatric Disease Annotations & Medicines


	chondroblastoma

Disease ID	919
Disease	chondroblastoma
Definition	A usually benign tumor composed of cells which arise from chondroblasts or their precursors and which tend to differentiate into cartilage cells. It occurs primarily in the epiphyses of adolescents. It is relatively rare and represents less than 2% of all primary bone tumors. The peak incidence is in the second decade of life; it is about twice as common in males as in females. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1846)
Synonym	[m]chondroblastoma nos [m]chondroblastoma nos (morphologic abnormality) chondroblastoma (morphologic abnormality) chondroblastoma [disease/finding] chondroblastoma morphology chondroblastoma of bone chondroblastoma of bone (disorder) chondroblastoma, nos chondroblastomas chondromatous giant cell tumor chondromatous giant cell tumour codman's tumor codman's tumour
DOID	DOID:2649
UMLS	C0008441
MeSH	D002804
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:11) C0017525 \| giant cell tumor \| 3 C0936248 \| chondroma \| 1 C0026764 \| myeloma \| 1 C0259779 \| fibrous dysplasia \| 1 C0002448 \| adamantinoma \| 1 C0153676 \| pulmonary metastasis \| 1 C0017525 \| giant cell tumors \| 1 C0025286 \| meningioma \| 1 C0153676 \| lung metastases \| 1 C0334605 \| meningothelial meningioma \| 1 C0008479 \| chondrosarcoma \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) H3F3B \| 3021 \| CTD_human
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:76) 7431 \| VIM \| DISEASES 3381 \| IBSP \| DISEASES 55907 \| CMAS \| DISEASES 6678 \| SPARC \| DISEASES 8600 \| TNFSF11 \| DISEASES 6662 \| SOX9 \| DISEASES 9098 \| USP6 \| DISEASES 968 \| CD68 \| DISEASES 3021 \| H3F3B \| DISEASES 3417 \| IDH1 \| DISEASES 3685 \| ITGAV \| DISEASES 4069 \| LYZ \| DISEASES 506 \| ATP5B \| DISEASES 6598 \| SMARCB1 \| DISEASES 1462 \| VCAN \| DISEASES 1009 \| CDH11 \| DISEASES 7157 \| TP53 \| DISEASES 6715 \| SRD5A1 \| DISEASES 85417 \| CCNB3 \| DISEASES 56934 \| CA10 \| DISEASES 56896 \| DPYSL5 \| DISEASES 3099 \| HK2 \| DISEASES 3856 \| KRT8 \| DISEASES 10630 \| PDPN \| DISEASES 2487 \| FRZB \| DISEASES 3549 \| IHH \| DISEASES 107 \| ADCY1 \| DISEASES 4982 \| TNFRSF11B \| DISEASES 84790 \| TUBA1C \| DISEASES 50964 \| SOST \| DISEASES 121340 \| SP7 \| DISEASES 214 \| ALCAM \| DISEASES 7534 \| YWHAZ \| DISEASES 947 \| CD34 \| DISEASES 5745 \| PTH1R \| DISEASES 221937 \| FOXK1 \| DISEASES 64764 \| CREB3L2 \| DISEASES 71 \| ACTG1 \| DISEASES 3418 \| IDH2 \| DISEASES 8338 \| HIST2H2AC \| DISEASES 23583 \| SMUG1 \| DISEASES 7430 \| EZR \| DISEASES 203068 \| TUBB \| DISEASES 4602 \| MYB \| DISEASES 875 \| CBS \| DISEASES 55107 \| ANO1 \| DISEASES 5265 \| SERPINA1 \| DISEASES 728378 \| POTEF \| DISEASES 9332 \| CD163 \| DISEASES 1284 \| COL4A2 \| DISEASES 800 \| CALD1 \| DISEASES 3020 \| H3F3A \| DISEASES 632 \| BGLAP \| DISEASES 6273 \| S100A2 \| DISEASES 6280 \| S100A9 \| DISEASES 8349 \| HIST2H2BE \| DISEASES 8337 \| HIST2H2AA3 \| DISEASES 5236 \| PGM1 \| DISEASES 860 \| RUNX2 \| DISEASES 546 \| ATRX \| DISEASES 3339 \| HSPG2 \| DISEASES 7692 \| ZNF133 \| DISEASES 2131 \| EXT1 \| DISEASES 54880 \| BCOR \| DISEASES 7280 \| TUBB2A \| DISEASES 10771 \| ZMYND11 \| DISEASES 114899 \| C1QTNF3 \| DISEASES 6736 \| SRY \| DISEASES 12 \| SERPINA3 \| DISEASES 5744 \| PTHLH \| DISEASES 176 \| ACAN \| DISEASES 7033 \| TFF3 \| DISEASES 100288687 \| DUX4 \| DISEASES 653545 \| DUX4L5 \| DISEASES 8792 \| TNFRSF11A \| DISEASES 103164619 \| PCAT2 \| DISEASES
Locus	(Waiting for update.)

Disease ID	919
Disease	chondroblastoma
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:9) HP:0012062 \| Bone cysts \| 9 HP:0012063 \| Aneurysmal bone cyst \| 8 HP:0002829 \| Arthralgias \| 1 HP:0002835 \| Aspiration \| 1 HP:0002756 \| Pathologic fracture \| 1 HP:0002664 \| Neoplasia \| 1 HP:0002858 \| Mengiomia \| 1 HP:0011847 \| Giant cell tumor of bone \| 1 HP:0006765 \| Chondrosarcoma \| 1

Disease ID	919
Disease	chondroblastoma
Manually Symptom	UMLS \| Name(Total Manually Symptoms:6) C1608408 \| malignant transformation C0277792 \| pathognomonic sign C0238790 \| bone destruction C0031111 \| periostitis C0017525 \| giant cell tumour C0002793 \| anaplastic change
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:1) C1608408 \| malignant transformation \| 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.)

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