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encyclopedia of Rare Disease Annotation for Precision Medicine

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	chondroma

Disease ID	1496
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	DOID:2602
UMLS	C0936248
MeSH	D002812
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:5) C0020492 \| hyperostosis \| 1 C0008441 \| chondroblastoma \| 1 C0879615 \| stromal tumor \| 1 C0029423 \| osteochondroma \| 1 C0238198 \| gastrointestinal stromal tumor \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:2) 3417 \| IDH1 \| CTD_human 3418 \| IDH2 \| CTD_human
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:28) 55107 \| ANO1 \| 2.689 \| DISEASES 1649 \| DDIT3 \| 1.053 \| DISEASES 1879 \| EBF1 \| 2.066 \| DISEASES 2131 \| EXT1 \| 2.649 \| DISEASES 2209 \| FCGR1A \| 1.299 \| DISEASES 2213 \| FCGR2B \| 1.44 \| DISEASES 2214 \| FCGR3A \| 1.534 \| DISEASES 2246 \| FGF1 \| 1.424 \| DISEASES 5348 \| FXYD1 \| 2.159 \| DISEASES 2591 \| GALNT3 \| 3.573 \| DISEASES 3052 \| HCCS \| 1.276 \| DISEASES 8091 \| HMGA2 \| 3.362 \| DISEASES 84525 \| HOPX \| 2.413 \| DISEASES 3303 \| HSPA1A \| 1.343 \| DISEASES 3316 \| HSPB2 \| 1.006 \| DISEASES 3418 \| IDH2 \| 1.254 \| DISEASES 3778 \| KCNMA1 \| 1.64 \| DISEASES 10186 \| LHFP \| 3.785 \| DISEASES 4193 \| MDM2 \| 1.409 \| DISEASES 4507 \| MTAP \| 2.073 \| DISEASES 4781 \| NFIB \| 2.344 \| DISEASES 5745 \| PTH1R \| 4.467 \| DISEASES 6390 \| SDHB \| 3.576 \| DISEASES 6391 \| SDHC \| 2.511 \| DISEASES 6392 \| SDHD \| 3.358 \| DISEASES 6441 \| SFTPD \| 1.661 \| DISEASES 7042 \| TGFB2 \| 1.132 \| DISEASES 51341 \| ZBTB7A \| 2.473 \| DISEASES
Locus	(Waiting for update.)

Disease ID	1496
Disease	chondroma
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:8) HP:0100723 \| Gastrointestinal stroma tumor \| 2 HP:0030431 \| Osteochondromas \| 1 HP:0040184 \| Oral hemorrhage \| 1 HP:0100774 \| Hyperostosis \| 1 HP:0000175 \| Palatoschisis \| 1 HP:0030432 \| Chondroblastoma \| 1 HP:0100246 \| Osteoma \| 1 HP:0002664 \| Neoplasia \| 1

Disease ID	1496
Disease	chondroma
Manually Symptom	UMLS \| Name(Total Manually Symptoms:1) C1608408 \| malignant transformation
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:1) C1608408 \| malignant transformation \| 1

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

Text Mining Genotype(Total 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.)

Disease ID	1496
Disease	chondroma
Case	(Waiting for update.)

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