PedAM

Pediatric Disease Annotations & Medicines


	osteoblastoma

Disease ID	920
Disease	osteoblastoma
Definition	A benign, painful, tumor of bone characterized by the formation of osteoid tissue, primitive bone and calcified tissue. It occurs frequently in the spine of young persons. (From Dorland, 27th ed; Stedman, 25th ed)
Synonym	[m]osteoblastoma fibroma, osteogenic, of bone giant osteoid osteoma giant osteoid osteomas ossifying giant cell tumor osteoblastoma (morphologic abnormality) osteoblastoma [disease/finding] osteoblastoma, benign osteoblastoma, nos osteoblastomas osteoid osteoma, giant osteoid osteomas, giant osteoma, giant osteoid osteomas, giant osteoid
Orphanet	ORPHANET:58040
DOID	DOID:0060098
UMLS	C0029417
MeSH	D018215
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:2) C0036440 \| idiopathic scoliosis \| 1 C0022739 \| klippel-trenaunay-weber syndrome \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:61) 84245 \| MRI1 \| DISEASES 54 \| ACP5 \| DISEASES 7431 \| VIM \| DISEASES 3381 \| IBSP \| DISEASES 3312 \| HSPA8 \| DISEASES 6678 \| SPARC \| DISEASES 471 \| ATIC \| DISEASES 6662 \| SOX9 \| DISEASES 9098 \| USP6 \| DISEASES 8140 \| SLC7A5 \| DISEASES 506 \| ATP5B \| DISEASES 8312 \| AXIN1 \| DISEASES 9368 \| SLC9A3R1 \| DISEASES 1009 \| CDH11 \| DISEASES 81631 \| MAP1LC3B \| DISEASES 1000 \| CDH2 \| DISEASES 7157 \| TP53 \| DISEASES 7345 \| UCHL1 \| DISEASES 107 \| ADCY1 \| DISEASES 84790 \| TUBA1C \| DISEASES 121340 \| SP7 \| DISEASES 4330 \| MN1 \| DISEASES 1051 \| CEBPB \| DISEASES 7534 \| YWHAZ \| DISEASES 2146 \| EZH2 \| DISEASES 8408 \| ULK1 \| DISEASES 6794 \| STK11 \| DISEASES 5499 \| PPP1CA \| DISEASES 64764 \| CREB3L2 \| DISEASES 5155 \| PDGFB \| DISEASES 83999 \| KREMEN1 \| DISEASES 71 \| ACTG1 \| DISEASES 5501 \| PPP1CC \| DISEASES 23583 \| SMUG1 \| DISEASES 7430 \| EZR \| DISEASES 203068 \| TUBB \| DISEASES 1499 \| CTNNB1 \| DISEASES 5154 \| PDGFA \| DISEASES 4745 \| NELL1 \| DISEASES 728378 \| POTEF \| DISEASES 5742 \| PTGS1 \| DISEASES 51438 \| MAGEC2 \| DISEASES 800 \| CALD1 \| DISEASES 5321 \| PLA2G4A \| DISEASES 5743 \| PTGS2 \| DISEASES 632 \| BGLAP \| DISEASES 117145 \| THEM4 \| DISEASES 860 \| RUNX2 \| DISEASES 3303 \| HSPA1A \| DISEASES 7692 \| ZNF133 \| DISEASES 7280 \| TUBB2A \| DISEASES 9350 \| CER1 \| DISEASES 192668 \| CYS1 \| DISEASES 6696 \| SPP1 \| DISEASES 2081 \| ERN1 \| DISEASES 862 \| RUNX1T1 \| DISEASES 5515 \| PPP2CA \| DISEASES 100506742 \| CASP12 \| DISEASES 83857 \| TMTC1 \| DISEASES 84133 \| ZNRF3 \| DISEASES 1649 \| DDIT3 \| DISEASES
Locus	(Waiting for update.)

Disease ID	920
Disease	osteoblastoma
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:5) HP:0012062 \| Bone cysts \| 6 HP:0012063 \| Aneurysmal bone cyst \| 6 HP:0100246 \| Osteoma \| 3 HP:0012531 \| Pain \| 1 HP:0001730 \| Progressive hearing impairment \| 1

Disease ID	920
Disease	osteoblastoma
Manually Symptom	UMLS \| Name(Total Manually Symptoms:1) C1608408 \| malignant transformation
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:1) C1608408 \| malignant transformation \| 2

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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