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PedAM

Pediatric Disease Annotations & Medicines



   juvenile pilocytic astrocytoma
  

Disease ID 912
Disease juvenile pilocytic astrocytoma
Definition
A slow-growing type of central nervous system tumor that forms from glial (supportive) tissue of the brain and spinal cord. Juvenile pilocytic astrocytoma usually occurs in children and young adults. It forms in the brain more often than the spinal cord.
Synonym
astrocytoma, juvenile pilocytic
astrocytomas, juvenile pilocytic
juvenile pilocytic astrocytomas
pilocytic astrocytoma, juvenile
pilocytic astrocytomas, juvenile
DOID
UMLS
C0280783
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:1)
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:18)
2026  |  ENO2  |  DISEASES
6945  |  MLX  |  DISEASES
2670  |  GFAP  |  DISEASES
2247  |  FGF2  |  DISEASES
7078  |  TIMP3  |  DISEASES
7157  |  TP53  |  DISEASES
55768  |  NGLY1  |  DISEASES
558  |  AXL  |  DISEASES
5604  |  MAP2K1  |  DISEASES
3643  |  INSR  |  DISEASES
80381  |  CD276  |  DISEASES
4978  |  OPCML  |  DISEASES
4763  |  NF1  |  DISEASES
4155  |  MBP  |  DISEASES
1654  |  DDX3X  |  DISEASES
1029  |  CDKN2A  |  DISEASES
50863  |  NTM  |  DISEASES
26137  |  ZBTB20  |  DISEASES
Locus(Waiting for update.)
Disease ID 912
Disease juvenile pilocytic astrocytoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:2)
Disease ID 912
Disease juvenile pilocytic astrocytoma
Manually Symptom
UMLS  | Name(Total Manually Symptoms:1)
C0018784  |  sensorineural hearing loss
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
rs11348802220806365673BRAFumls:C0280783BeFreeAZD6244 was evaluated against two JPA xenografts, BT-35 (wild-type BRAF) and BT-40 (mutant [V600E] BRAF).0.0002714422010BRAF7140753336AT,G,C
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0000407Sensorineural hearing impairmentMP:0006330syndromic hearing impairment;
Mapped by homologous gene(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0000407Sensorineural hearing impairmentMP:0000010abnormal abdominal fat pad morphology;
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.)