PedAM

Pediatric Disease Annotations & Medicines


	childhood medulloblastoma

Disease ID	1440
Disease	childhood medulloblastoma
Definition	A medulloblastoma occurring in children.
Synonym	brain tumor, child: medulloblastoma cerebellar pnet, childhood cerebellar pnet, pediatric cerebellar primitive neuroectodermal tumor, childhood cerebellar primitive neuroectodermal tumor, pediatric cerebellar, childhood, pnet cerebellar, pediatric, pnet childhood cerebellar pnet childhood cerebellar primitive neuroectodermal tumor childhood infratentorial pnet childhood infratentorial primitive neuroectodermal tumor childhood medulloblastomas infratentorial pnet, childhood infratentorial pnet, pediatric infratentorial primitive neuroectodermal tumor, childhood infratentorial primitive neuroectodermal tumor, pediatric infratentorial, childhood, pnet infratentorial, pediatric, pnet medulloblastoma, childhood medulloblastoma, pediatric medulloblastomas, childhood pediatric cerebellar pnet pediatric cerebellar primitive neuroectodermal tumor pediatric infratentorial pnet pediatric infratentorial primitive neuroectodermal tumor pediatric medulloblastoma pnet, cerebellar, childhood pnet, cerebellar, pediatric pnet, childhood cerebellar pnet, childhood infratentorial pnet, infratentorial, childhood pnet, infratentorial, pediatric pnet, pediatric cerebellar pnet, pediatric infratentorial primitive neuroectodermal tumor, childhood cerebellar primitive neuroectodermal tumor, childhood infratentorial primitive neuroectodermal tumor, pediatric cerebellar primitive neuroectodermal tumor, pediatric infratentorial
DOID	DOID:3869
UMLS	C0278510
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:4) C0021390 \| inflammatory bowel disease \| 1 C0009241 \| cognitive disorders \| 1 C0002170 \| alopecia \| 1 C0021831 \| bowel disease \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:88) 100048912 \| CDKN2B-AS1 \| DISEASES 9423 \| NTN1 \| DISEASES 771 \| CA12 \| DISEASES 4741 \| NEFM \| DISEASES 2735 \| GLI1 \| DISEASES 6659 \| SOX4 \| DISEASES 2670 \| GFAP \| DISEASES 56112 \| PCDHGA3 \| DISEASES 79727 \| LIN28A \| DISEASES 4853 \| NOTCH2 \| DISEASES 4659 \| PPP1R12A \| DISEASES 51528 \| JKAMP \| DISEASES 894 \| CCND2 \| DISEASES 4756 \| NEO1 \| DISEASES 9727 \| RAB11FIP3 \| DISEASES 1031 \| CDKN2C \| DISEASES 6855 \| SYP \| DISEASES 2034 \| EPAS1 \| DISEASES 84083 \| ZRANB3 \| DISEASES 5244 \| ABCB4 \| DISEASES 79109 \| MAPKAP1 \| DISEASES 2065 \| ERBB3 \| DISEASES 84530 \| SRRM4 \| DISEASES 10351 \| ABCA8 \| DISEASES 7157 \| TP53 \| DISEASES 2064 \| ERBB2 \| DISEASES 6455 \| SH3GL1 \| DISEASES 10733 \| PLK4 \| DISEASES 2052 \| EPHX1 \| DISEASES 4613 \| MYCN \| DISEASES 6317 \| SERPINB3 \| DISEASES 9947 \| MAGEC1 \| DISEASES 54361 \| WNT4 \| DISEASES 9442 \| MED27 \| DISEASES 27306 \| HPGDS \| DISEASES 6469 \| SHH \| DISEASES 5347 \| PLK1 \| DISEASES 10653 \| SPINT2 \| DISEASES 116071 \| BATF2 \| DISEASES 4255 \| MGMT \| DISEASES 4744 \| NEFH \| DISEASES 2688 \| GH1 \| DISEASES 23212 \| RRS1 \| DISEASES 6664 \| SOX11 \| DISEASES 3714 \| JAG2 \| DISEASES 5727 \| PTCH1 \| DISEASES 219699 \| UNC5B \| DISEASES 283093 \| OR4C12 \| DISEASES 2066 \| ERBB4 \| DISEASES 79632 \| FAM184A \| DISEASES 1499 \| CTNNB1 \| DISEASES 10533 \| ATG7 \| DISEASES 51155 \| HN1 \| DISEASES 3084 \| NRG1 \| DISEASES 22931 \| RAB18 \| DISEASES 6752 \| SSTR2 \| DISEASES 6597 \| SMARCA4 \| DISEASES 4916 \| NTRK3 \| DISEASES 7150 \| TOP1 \| DISEASES 2736 \| GLI2 \| DISEASES 116496 \| FAM129A \| DISEASES 59336 \| PRDM13 \| DISEASES 51684 \| SUFU \| DISEASES 115209 \| OMA1 \| DISEASES 2048 \| EPHB2 \| DISEASES 9696 \| CROCC \| DISEASES 7546 \| ZIC2 \| DISEASES 3604 \| TNFRSF9 \| DISEASES 4609 \| MYC \| DISEASES 7020 \| TFAP2A \| DISEASES 8618 \| CADPS \| DISEASES 2068 \| ERCC2 \| DISEASES 55054 \| ATG16L1 \| DISEASES 655 \| BMP7 \| DISEASES 2737 \| GLI3 \| DISEASES 1654 \| DDX3X \| DISEASES 1994 \| ELAVL1 \| DISEASES 2011 \| MARK2 \| DISEASES 56616 \| DIABLO \| DISEASES 8522 \| GAS7 \| DISEASES 340371 \| NRBP2 \| DISEASES 8842 \| PROM1 \| DISEASES 9140 \| ATG12 \| DISEASES 2053 \| EPHX2 \| DISEASES 586 \| BCAT1 \| DISEASES 101 \| ADAM8 \| DISEASES 126520 \| PLK5 \| DISEASES 26806 \| SNORD44 \| DISEASES
Locus	(Waiting for update.)

Disease ID	1440
Disease	childhood medulloblastoma
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:2) HP:0002664 \| Neoplasia \| 2 HP:0001596 \| Hair loss \| 1

Disease ID	1440
Disease	childhood medulloblastoma
Manually Symptom	UMLS \| Name(Total Manually Symptoms:1) C0027627 \| secondary malignancies
Text Mined Symptom	(Waiting for update.)

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

All Snps(Total Genotypes:1)
snpId	pubmedId	geneId	geneSymbol	diseaseId	sourceId	sentence	score	Year	geneSymbol_dbSNP	CHROMOSOME	POS	REF	ALT
rs1695	23065688	26768	SNORA73B	umls:C0278510	BeFree	We explored the relationship between the host GSTP1 105 A > G polymorphism (rs1695), tumor GSTpi protein expression, and clinical outcomes in pediatric medulloblastoma.	0.000271442	2013	GSTP1	11	67585218	A	G

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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