Neuroblastoma
Description
Neuroblastoma is a malignant tumor of neural crest cells, the cells that give rise to the sympathetic nervous system, which is observed in children.
Genes related to Neuroblastoma
- ALK
 - KIF1B
 - PIK3CA
 - PTPN11
 - FGFR1
 - MYCN
 - PHOX2B
 - TP53
 - HACE1
 - LIN28B
 - LMO1
 - TOP2A
 - NME1
 - MYC
 
Clinical Features
Top most frequent phenotypes and symptoms related to Neuroblastoma
- Ataxia
 - Neoplasm
 - Failure to thrive
 - Pain
 - Anemia
 - Hypertension
 - Fever
 - Diarrhea
 - Myoclonus
 - Abdominal pain
 
And another 20 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Based on the latest data available NEUROBLASTOMA have a estimated incidence of 1.26 per 100k in Europe.— No data available about the known clinical features onset.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Neuroblastoma Recommended genes panels
| Panel Name, Specifity and genes Tested/covered | 
|---|
 	Hereditary Brain, CNS, PNS Cancer Panel.
By Baylor Miraca Genetics Laboratories (United States). 
TP53, VHL, SUFU, PALB2, ALK, APC, MEN1, MLH1, MRE11, MSH2, MSH6, NBN, NF2, ATM, PMS2, PHOX2B, PTCH1
 
Specificity
 
18 % 
Genes
 
22 %  | 
 	Hereditary Brain, CNS, PNS Cancer Panel.
By Baylor Miraca Genetics Laboratories (United States). 
TP53, VHL, SUFU, PALB2, ALK, APC, MEN1, MLH1, MRE11, MSH2, MSH6, NBN, NF2, ATM, PMS2, PHOX2B, PTCH1
 
Specificity
 
18 % 
Genes
 
22 %  | 
 	Comprehensive Hereditary Cancer Panel.
By Baylor Miraca Genetics Laboratories (United States). 
RUNX1, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRCA1, BRCA2, STK11, EPCAM, TP53, VHL, WT1, CBL, SUFU, CDC73, CDH1, CDK4, CDKN1C, CDKN2A	, (...)
 
View the complete list with 39 more genes 
Specificity
 
7 % 
Genes
 
29 %  | 
 	VistaSeq Brain/CNS/PNS Cancer Panel.
By Molecular Diagnostic Laboratory University of Alberta (Canada). 
SMARCB1, TP53, VHL, SUFU, ALK, APC, MEN1, MLH1, MSH2, MSH6, NBN, NF1, NF2, PMS2, PHOX2B, PTCH1, RB1
 
Specificity
 
18 % 
Genes
 
22 %  | 
 	Hereditary Cancer Panel, Sequencing and Deletion/Duplication.
By ARUP Laboratories, Molecular Genetics and Genomics (United States). 
SDHB, SDHC, SDHD, BMPR1A, BRCA1, BRCA2, SMARCB1, STK11, EPCAM, TP53, TSC1, TSC2, VHL, SUFU, CDH1, CDK4, CDKN1B, CDKN2A, BRIP1, SDHAF2	, (...)
 
View the complete list with 26 more genes 
Specificity
 
7 % 
Genes
 
22 %  | 
 	Hereditary Cancer Panel - Neuro17.
By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center (United States). 
TP53, TSC1, TSC2, VHL, SUFU, ALK, APC, MEN1, MLH1, MSH2, MSH6, NBN, NF1, NF2, PMS2, PHOX2B, PTCH1
 
Specificity
 
18 % 
Genes
 
22 %  | 
 	Hereditary Cancer Panel- Comprehensive63.
By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center (United States). 
BLM, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRCA1, BRCA2, SMARCA4, STK11, EPCAM, TP53, TSC1, TSC2, VHL, XRCC2, SUFU, CDC73, DICER1, CDH1	, (...)
 
View the complete list with 42 more genes 
Specificity
 
5 % 
Genes
 
22 %  | 
 	BrainTumorNext.
By Ambry Genetics (United States). 
SMARCA4, SMARCB1, SMARCE1, TP53, TSC1, TSC2, VHL, SUFU, DICER1, POT1, CDKN1B, CDKN2A, AIP, ALK, APC, MEN1, MLH1, MSH2, MSH6, NBN	, (...)
 
View the complete list with 7 more genes 
Specificity
 
12 % 
Genes
 
22 %  | 
You can get up to 1000 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
ORPHANET OMIM Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like NEPHROGENIC DIABETES INSIPIDUS CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iy; CDG1Y HYPERTENSION AND BRACHYDACTYLY SYNDROME; HTNB CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13 ALBINISM, OCULOCUTANEOUS, TYPE IB; OCA1B DIABETES MELLITUS, TRANSIENT NEONATAL, 2
	Hereditary Brain, CNS, PNS Cancer Panel.
	VistaSeq Brain/CNS/PNS Cancer Panel.