PedAM

Pediatric Disease Annotations & Medicines


	fibroma

Disease ID	1506
Disease	fibroma
Definition	A benign tumor of fibrous or fully developed connective tissue.
Synonym	[m]fibroma nos [m]fibroma nos (morphologic abnormality) fibroma (disorder) fibroma [disease/finding] fibroma durum fibroma, benign fibroma, no icd-o subtype fibroma, no icd-o subtype (morphologic abnormality) fibroma, no international classification of diseases for oncology subtype fibroma, no international classification of diseases for oncology subtype (morphologic abnormality) fibroma, nos fibromas fibrous tissue tumor
DOID	DOID:0050871
UMLS	C0016045
MeSH	D005350
SNOMED-CT	SNOMEDCT_US_2016_09_01:424568000
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:30) C0206640 \| cementifying fibroma \| 2 C0017525 \| giant cell tumor \| 2 C1334699 \| mesenchymal tumor \| 1 C0004779 \| gorlin syndrome \| 1 C0547030 \| visual disturbance \| 1 C0042133 \| uterine myoma \| 1 C0018206 \| granulosa cell tumor \| 1 C0022658 \| renal disease \| 1 C0334121 \| inflammatory pseudotumor \| 1 C0020502 \| hyperparathyroidism \| 1 C0027858 \| neuroma \| 1 C0086692 \| benign neoplasm \| 1 C0302592 \| carcinoma cervix \| 1 C0021933 \| intussusception \| 1 C0018922 \| haemangiopericytoma \| 1 C0879615 \| stromal tumor \| 1 C0022658 \| renal diseases \| 1 C0010633 \| cystadenoma \| 1 C0018818 \| ventricular septal defect \| 1 C0878500 \| epithelial dysplasia \| 1 C0016057 \| fibrosarcoma \| 1 C0346010 \| birt-hogg-dube syndrome \| 1 C0018206 \| granulosa cell tumors \| 1 C0086692 \| benign neoplasms \| 1 C0029423 \| osteochondroma \| 1 C0346170 \| serous cystadenoma of the ovary \| 1 C0007194 \| hypertrophic cardiomyopathy \| 1 C0029463 \| osteosarcoma \| 1 C0022661 \| end-stage renal disease \| 1 C0259779 \| fibrous dysplasia \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:2) GRM1 \| 2911 \| CTD_human ANTXR2 \| 118429 \| CTD_human
Inferring Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) 1499 \| CTNNB1 \| infer
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:151) 3861 \| KRT14 \| DISEASES 54474 \| KRT20 \| DISEASES 7145 \| TNS1 \| DISEASES 266 \| AMELY \| DISEASES 7249 \| TSC2 \| DISEASES 8976 \| WASL \| DISEASES 7431 \| VIM \| DISEASES 1277 \| COL1A1 \| DISEASES 595 \| CCND1 \| DISEASES 4254 \| KITLG \| DISEASES 84519 \| ACRBP \| DISEASES 2026 \| ENO2 \| DISEASES 2822 \| GPLD1 \| DISEASES 4012 \| LNPEP \| DISEASES 84141 \| EVA1A \| DISEASES 4317 \| MMP8 \| DISEASES 8074 \| FGF23 \| DISEASES 27230 \| SERP1 \| DISEASES 4656 \| MYOG \| DISEASES 3229 \| HOXC13 \| DISEASES 1300 \| COL10A1 \| DISEASES 2069 \| EREG \| DISEASES 6662 \| SOX9 \| DISEASES 3860 \| KRT13 \| DISEASES 4654 \| MYOD1 \| DISEASES 9098 \| USP6 \| DISEASES 968 \| CD68 \| DISEASES 6299 \| SALL1 \| DISEASES 3852 \| KRT5 \| DISEASES 3866 \| KRT15 \| DISEASES 2521 \| FUS \| DISEASES 3021 \| H3F3B \| DISEASES 23175 \| LPIN1 \| DISEASES 23314 \| SATB2 \| DISEASES 7597 \| ZBTB25 \| DISEASES 9739 \| SETD1A \| DISEASES 6598 \| SMARCB1 \| DISEASES 10874 \| NMU \| DISEASES 1009 \| CDH11 \| DISEASES 7157 \| TP53 \| DISEASES 5868 \| RAB5A \| DISEASES 740 \| MRPL49 \| DISEASES 55079 \| FEZF2 \| DISEASES 201163 \| FLCN \| DISEASES 3815 \| KIT \| DISEASES 4690 \| NCK1 \| DISEASES 6285 \| S100B \| DISEASES 1584 \| CYP11B1 \| DISEASES 3856 \| KRT8 \| DISEASES 6228 \| RPS23 \| DISEASES 1669 \| DEFA4 \| DISEASES 7373 \| COL14A1 \| DISEASES 22974 \| TPX2 \| DISEASES 121340 \| SP7 \| DISEASES 1140 \| CHRNB1 \| DISEASES 260434 \| PYDC1 \| DISEASES 118429 \| ANTXR2 \| DISEASES 2119 \| ETV5 \| DISEASES 794 \| CALB2 \| DISEASES 27087 \| B3GAT1 \| DISEASES 3054 \| HCFC1 \| DISEASES 947 \| CD34 \| DISEASES 8061 \| FOSL1 \| DISEASES 258 \| AMBN \| DISEASES 4684 \| NCAM1 \| DISEASES 10938 \| EHD1 \| DISEASES 10611 \| PDLIM5 \| DISEASES 5745 \| PTH1R \| DISEASES 3039 \| HBA1 \| DISEASES 4312 \| MMP1 \| DISEASES 6794 \| STK11 \| DISEASES 5241 \| PGR \| DISEASES 1303 \| COL12A1 \| DISEASES 1668 \| DEFA3 \| DISEASES 221937 \| FOXK1 \| DISEASES 64764 \| CREB3L2 \| DISEASES 3855 \| KRT7 \| DISEASES 5155 \| PDGFB \| DISEASES 7490 \| WT1 \| DISEASES 3418 \| IDH2 \| DISEASES 5727 \| PTCH1 \| DISEASES 668 \| FOXL2 \| DISEASES 4221 \| MEN1 \| DISEASES 23583 \| SMUG1 \| DISEASES 26578 \| OSTF1 \| DISEASES 401138 \| AMTN \| DISEASES 2804 \| GOLGB1 \| DISEASES 1499 \| CTNNB1 \| DISEASES 26762 \| HAVCR1 \| DISEASES 5325 \| PLAGL1 \| DISEASES 2335 \| FN1 \| DISEASES 55107 \| ANO1 \| DISEASES 5265 \| SERPINA1 \| DISEASES 2074 \| ERCC6 \| DISEASES 219844 \| HYLS1 \| DISEASES 10298 \| PAK4 \| DISEASES 9332 \| CD163 \| DISEASES 1284 \| COL4A2 \| DISEASES 4311 \| MME \| DISEASES 4519 \| MT-CYB \| DISEASES 23499 \| MACF1 \| DISEASES 800 \| CALD1 \| DISEASES 3880 \| KRT19 \| DISEASES 3020 \| H3F3A \| DISEASES 5788 \| PTPRC \| DISEASES 79577 \| CDC73 \| DISEASES 1660 \| DHX9 \| DISEASES 10763 \| NES \| DISEASES 2444 \| FRK \| DISEASES 6273 \| S100A2 \| DISEASES 6278 \| S100A7 \| DISEASES 6280 \| S100A9 \| DISEASES 3713 \| IVL \| DISEASES 5016 \| OVGP1 \| DISEASES 7272 \| TTK \| DISEASES 5236 \| PGM1 \| DISEASES 2778 \| GNAS \| DISEASES 5728 \| PTEN \| DISEASES 9562 \| MINPP1 \| DISEASES 2516 \| NR5A1 \| DISEASES 4303 \| FOXO4 \| DISEASES 7088 \| TLE1 \| DISEASES 8573 \| CASK \| DISEASES 116840 \| CNTROB \| DISEASES 265 \| AMELX \| DISEASES 4267 \| CD99 \| DISEASES 2315 \| MLANA \| DISEASES 1667 \| DEFA1 \| DISEASES 728358 \| DEFA1B \| DISEASES 388698 \| FLG2 \| DISEASES 3875 \| KRT18 \| DISEASES 55576 \| STAB2 \| DISEASES 6370 \| CCL25 \| DISEASES 12 \| SERPINA3 \| DISEASES 3161 \| HMMR \| DISEASES 64400 \| AKTIP \| DISEASES 10117 \| ENAM \| DISEASES 54959 \| ODAM \| DISEASES 8091 \| HMGA2 \| DISEASES 23414 \| ZFPM2 \| DISEASES 3481 \| IGF2 \| DISEASES 23210 \| JMJD6 \| DISEASES 1029 \| CDKN2A \| DISEASES 387836 \| CLEC2A \| DISEASES 2130 \| EWSR1 \| DISEASES 389549 \| FEZF1 \| DISEASES 339487 \| ZBTB8OS \| DISEASES 90993 \| CREB3L1 \| DISEASES 9774 \| BCLAF1 \| DISEASES 3851 \| KRT4 \| DISEASES 378805 \| LINC-PINT \| DISEASES
Locus	(Waiting for update.)

Disease ID	1506
Disease	fibroma
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:30) HP:0012062 \| Bone cysts \| 10 HP:0012063 \| Aneurysmal bone cyst \| 9 HP:0001541 \| Ascites \| 7 HP:0030426 \| Ossifying fibroma \| 4 HP:0002664 \| Neoplasia \| 4 HP:0004756 \| Ventricular tachycardia \| 2 HP:0001629 \| Ventricular septal defects \| 1 HP:0030430 \| Pinched nerve \| 1 HP:0003774 \| End-stage renal failure \| 1 HP:0001571 \| Impacted teeth \| 1 HP:0030431 \| Osteochondromas \| 1 HP:0001649 \| Tachycardia \| 1 HP:0430028 \| Increased size of maxilla \| 1 HP:0100246 \| Osteoma \| 1 HP:0030731 \| Carcinoma \| 1 HP:0002576 \| Intussusception \| 1 HP:0100244 \| Fibrosarcoma \| 1 HP:0001806 \| Oncholysis \| 1 HP:0011675 \| Arrhythmias \| 1 HP:0001012 \| Multiple lipomas \| 1 HP:0002669 \| Osteosarcoma \| 1 HP:0011847 \| Giant cell tumor of bone \| 1 HP:0001695 \| Cardiac arrest \| 1 HP:0002202 \| Pleural effusion \| 1 HP:0000843 \| Hyperparathyroidism \| 1 HP:0002027 \| Abdominal pain \| 1 HP:0012031 \| Lipomatous tumor \| 1 HP:0000718 \| Aggressive behaviour \| 1 HP:0030038 \| Enchondroma \| 1 HP:0001639 \| Hypertrophic cardiomyopathy \| 1

Disease ID	1506
Disease	fibroma
Manually Symptom	(Waiting for update.)
Text Mined Symptom	(Waiting for update.)

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:0)
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GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)

GWASdb Snp Trait(Total Genotypes:0)
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Mapped by lexical matching(Total Items:0)
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Mapped by homologous gene(Total Items:0)
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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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