PedAM

Pediatric Disease Annotations & Medicines


	congenital mesoblastic nephroma

Disease ID	1087
Disease	congenital mesoblastic nephroma
Definition	Congenital mesoblastic nephroma is a type of kidney tumor that is usually found before birth by ultrasound or within the first 3 months of life. It contains fibroblastic cells (connective tissue cells), and may spread to the other kidney or to nearby tissue. [HPO:sdoelken]
Synonym	congen mesoblastic nephroma congenital mesoblastic nephromas mesoblastic nephroma, congenital mesoblastic nephromas, congenital nephroma, congenital mesoblastic nephromas, congenital mesoblastic stromal nephroma, malignant
Orphanet	ORPHANET:2665
DOID	DOID:4773
UMLS	C1332965
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:2) NTRK3 \| 4916 \| ORPHANET ETV6 \| 2120 \| ORPHANET
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:30) 10857 \| PGRMC1 \| DISEASES 5266 \| PI3 \| DISEASES 10752 \| CHL1 \| DISEASES 7057 \| THBS1 \| DISEASES 6121 \| RPE65 \| DISEASES 6598 \| SMARCB1 \| DISEASES 10664 \| CTCF \| DISEASES 7531 \| YWHAE \| DISEASES 5546 \| PRCC \| DISEASES 5972 \| REN \| DISEASES 4613 \| MYCN \| DISEASES 5741 \| PTH \| DISEASES 178 \| AGL \| DISEASES 3251 \| HPRT1 \| DISEASES 4330 \| MN1 \| DISEASES 27087 \| B3GAT1 \| DISEASES 7030 \| TFE3 \| DISEASES 10611 \| PDLIM5 \| DISEASES 4094 \| MAF \| DISEASES 7490 \| WT1 \| DISEASES 4151 \| MB \| DISEASES 93034 \| NT5C1B \| DISEASES 4916 \| NTRK3 \| DISEASES 9846 \| GAB2 \| DISEASES 4893 \| NRAS \| DISEASES 4952 \| OCRL \| DISEASES 727837 \| SSX2B \| DISEASES 4267 \| CD99 \| DISEASES 2120 \| ETV6 \| DISEASES 3481 \| IGF2 \| DISEASES
Locus	Symbol \| Locus(Total Locus:2) ETV6 \| 12p13.2 NTRK3 \| 15q25.3

Disease ID	1087
Disease	congenital mesoblastic nephroma
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:2) HP:0000790 \| Hematuria \| 1 HP:0000086 \| Ectopic kidney \| 1

Disease ID	1087
Disease	congenital mesoblastic nephroma
Manually Symptom	UMLS \| Name(Total Manually Symptoms:2) C0020437 \| hypercalcemia C0020224 \| polyhydramnios
Text Mined Symptom	(Waiting for update.)

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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