Lymphoma, Non-hodgkin, Familial

Description

Non-Hodgkin malignant lymphomas(NHL) is a heterogeneous group of malignant tumors of the lymphoid system.

Clinical Features

Phenotypes and symptoms related to Lymphoma, Non-hodgkin, Familial

  • Neoplasm
  • Leukemia
  • Lymphoma
  • Hodgkin lymphoma
  • B-cell lymphoma
  • Chronic lymphatic leukemia
  • Non-Hodgkin lymphoma
  • T-cell lymphoma

Incidence and onset information

— Based on the latest data available Lymphoma, Non-hodgkin, Familial have a estimated incidence of 11.6 per 100k worldwide.


Mendelian

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Lymphoma, Non-hodgkin, Familial Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Mesothelioma, somatic.

By Centogene AG - the Rare Disease Company in Germany.

BCL10
Specificity
100 %
Genes
20 %
Lymphoma, MALT, somatic.

By Centogene AG - the Rare Disease Company in Germany.

BCL10
Specificity
100 %
Genes
20 %
Lymphoma, follicular, somatic.

By Centogene AG - the Rare Disease Company in Germany.

BCL10
Specificity
100 %
Genes
20 %
Male germ cell tumor, somatic.

By Centogene AG - the Rare Disease Company in Germany.

BCL10
Specificity
100 %
Genes
20 %
Invitae Comprehensive Severe Combined Immunodeficiency (SCID) and Combined Immunodeficiency (CID) Panel.

By Invitae in United States.

TAP1, AK2, ADA, IL2RG, PNP, DCLRE1C, MAGT1, DOCK8, JAK3, CD40LG, CD3E, CD3D, IL7R, RAG2, RAG1, ZAP70, ITK, RAC2, NHEJ1, LIG4 , (...)

View the complete list with 29 more genes
Specificity
3 %
Genes
20 %
Invitae Primary Immunodeficiency Panel.

By Invitae in United States.

PMS2, STAT1, SLC37A4, CASP8, TLR3, HAX1, AP3B1, UNG, TAP1, TAZ, TCN2, AK2, SLC35C1, CYBA, STAT3, ADA, MOGS, IL2RG, PNP, AIRE , (...)

View the complete list with 187 more genes
Specificity
2 %
Genes
60 %
Invitae Combined Immunodeficiency (CID) Panel.

By Invitae in United States.

TAP1, MAGT1, DOCK8, CD40LG, ZAP70, ITK, RAC2, LRBA, CD27, CIITA, RFX5, RFXANK, RFXAP, STK4, ICOS, CARD11, B2M, IL21, IL21R, MALT1 , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
20 %
BCL10.

By Fulgent Genetics Fulgent Genetics in United States.

BCL10
Specificity
100 %
Genes
20 %
Onco microarray for CLL.

By Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center in United States.

TP53, ALK, ATM, IGH, AKT1, ITK, CCND1, BCL2, BCL6, MYC, BCL11A, BCL10, MYBL1, MYB, FGF2, BCL3
Specificity
7 %
Genes
20 %
Primary Immunodeficiency Panel.

By Blueprint Genetics in Finland.

PMS2, RECQL4, STAT1, SLC37A4, CASP8, CLCN7, HAX1, AP3B1, UNG, TAP1, TCN2, AK2, SLC35C1, CYBA, STAT3, ADA, MOGS, IL2RG, PNP, AIRE , (...)

View the complete list with 255 more genes
Specificity
2 %
Genes
60 %
Focus::DLBCL&FL™ NGS Panel.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

PTEN, TP53, STAT3, BRAF, CREBBP, KRAS, ATM, CDKN2A, BTK, KMT2D, MTOR, NOTCH1, EZH2, ARID1A, EP300, TET2, MYD88, IKZF1, FAS, PIK3CD , (...)

View the complete list with 24 more genes
Specificity
3 %
Genes
20 %
Focus::Lymphoma™ NGS Panel.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

PTEN, TP53, STAT3, BRAF, CREBBP, KRAS, ATM, CDKN2A, BTK, KMT2D, MTOR, NOTCH1, EZH2, ARID1A, EP300, TET2, MYD88, IKZF1, FAS, PIK3CD , (...)

View the complete list with 29 more genes
Specificity
3 %
Genes
20 %
FoundationOne® Heme.

By Foundation Medicine, Inc. in United States.

BRCA1, BRCA2, VHL, APC, MSH2, MSH6, MLH1, MUTYH, PTEN, RUNX1, TP53, PC, FOXL2, HNF1A, WT1, RB1, RET, TNFRSF11A, CPS1, SDHC , (...)

View the complete list with 385 more genes
Specificity
1 %
Genes
20 %
Caris MI TumorSeek 592-Gene NGS Panel.

By Caris Life Sciences in United States.

BRCA1, BRCA2, VHL, APC, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, FOXL2, HNF1A, PPARG, COL1A1, WT1, RB1, SDHAF2 , (...)

View the complete list with 571 more genes
Specificity
1 %
Genes
40 %
Tempus xT assay.

By Tempus Labs, Inc. in United States.

BRCA1, BRCA2, MTHFR, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, ATP7B, FOXL2, HNF1A, WT1, RB1 , (...)

View the complete list with 571 more genes
Specificity
1 %
Genes
40 %
Tempus xO assay.

By Tempus Labs, Inc. in United States.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, ABCB11, ABCB4, FKBP10, FOXL2, HNF1A, PPARG , (...)

View the complete list with 1693 more genes
Specificity
1 %
Genes
80 %
RAD54B.

By Fulgent Genetics Fulgent Genetics in United States.

RAD54B
Specificity
100 %
Genes
20 %
Solid Tumor Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

BRCA1, BRCA2, VHL, APC, MLH1, PTEN, TP53, FOXL2, PPARG, WT1, RB1, RET, RAF1, IDH2, FGFR3, AR, BRAF, CREBBP, HRAS, KRAS , (...)

View the complete list with 102 more genes
Specificity
1 %
Genes
20 %
Breast Tumors Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

BRCA1, BRCA2, PTEN, RUNX1, TP53, RB1, RET, IDH2, BRAF, HRAS, KRAS, MAP2K1, FGFR2, MAP2K2, ATM, PALB2, CDH1, STK11, CDK4, CDKN2A , (...)

View the complete list with 22 more genes
Specificity
3 %
Genes
20 %
RAD54L.

By Fulgent Genetics Fulgent Genetics in United States.

RAD54L
Specificity
100 %
Genes
20 %
CASP10 Sequencing.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

CASP10
Specificity
100 %
Genes
20 %
Autoimmune Lymphoproliferative Syndrome Panel by next-generation sequencing (NGS).

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

CASP8, KRAS, NRAS, MAGT1, FAS, FASLG, CASP10, ITK, FADD
Specificity
12 %
Genes
20 %
Autoimmune Lymphoproliferative Syndrome Deletion/Duplication Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

CASP8, KRAS, NRAS, MAGT1, FAS, FASLG, CASP10, ITK, FADD
Specificity
12 %
Genes
20 %
CASP10 Deletion/duplication analysis.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

CASP10
Specificity
100 %
Genes
20 %
Tier 2: Hereditary Lymphoma and Immunodeficiency Panel.

By Genetic Services Laboratory University of Chicago in United States.

BRCA1, BRCA2, ADA, BLM, ATM, NBN, PRF1, WAS, NF1, MAGT1, DOCK8, SH2D1A, IKZF1, TNFRSF13B, FAS, FASLG, CASP10, STXBP2, ITK, PIK3CD , (...)

View the complete list with 3 more genes
Specificity
9 %
Genes
40 %
CASP10. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

CASP10
Specificity
100 %
Genes
20 %
Autoimmune lymphoproliferative syndrome type II (sequence analysis of CASP10 gene).

By CGC Genetics in Portugal.

CASP10
Specificity
100 %
Genes
20 %
Autoimmune Lymphoproliferative Syndrome/ALPS Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

CASP8, STAT3, KRAS, NRAS, MAGT1, SH2D1A, FAS, XIAP, FASLG, CASP10, ITK, PIK3CD, LRBA, FADD, CTLA4, PRKCD
Specificity
7 %
Genes
20 %
CASP10.

By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.

CASP10
Specificity
100 %
Genes
20 %
ALPS/autoimmunity panel.

By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.

CASP8, AIRE, KRAS, NRAS, FOXP3, FAS, FASLG, CASP10, LRBA, FADD, IL2RA, ITCH
Specificity
9 %
Genes
20 %
Autoimmune lymphoproliferative syndrome.

By Centogene AG - the Rare Disease Company in Germany.

CASP10
Specificity
100 %
Genes
20 %
Bone marrow failure syndromes with Leukemia Panel.

By CeGaT GmbH in Germany.

RUNX1, NBN, CEBPA, GATA1, CASP10
Specificity
20 %
Genes
20 %
Immune dysregulation Panel.

By CeGaT GmbH in Germany.

CASP8, AP3B1, AIRE, PRF1, TREX1, FOXP3, LYST, SH2D1A, RAB27A, UNC13D, FAS, STX11, XIAP, FASLG, CASP10, STXBP2, PRKCD, CARD11, IL2RA, ITCH , (...)

View the complete list with 2 more genes
Specificity
10 %
Genes
40 %
Invitae Monogenic Autoimmunity Panel.

By Invitae in United States.

STAT1, CASP8, AP3B1, UNG, CYBA, STAT3, PNP, AIRE, RMRP, PRF1, CYBB, SLC7A7, WAS, BTK, SAMHD1, RNASEH2A, RNASEH2C, RNASEH2B, TREX1, TBX1 , (...)

View the complete list with 53 more genes
Specificity
3 %
Genes
40 %
CASP10.

By Fulgent Genetics Fulgent Genetics in United States.

CASP10
Specificity
100 %
Genes
20 %
Autoimmune lymphoproliferative syndrome type 2A.

By Bioarray in Spain.

CASP10
Specificity
100 %
Genes
20 %
LYMPHOPROLIFERATIVE SYNDROME, AUTOIMMUNE.

By Laboratorio de Genetica Clinica SL in Spain.

CASP8, NRAS, FAS, FASLG, CASP10
Specificity
20 %
Genes
20 %
Autoimmune Lymphoproliferative Syndrome Type II, Sequencing CASP10 Gene.

By Reference Laboratory Genetics in Spain.

CASP10
Specificity
100 %
Genes
20 %
Autosomic Autoimmune Lymphoproliferative Syndrome , Panel Massive Sequencing (NGS) 10 Genes.

By Reference Laboratory Genetics in Spain.

CASP8, KRAS, NRAS, MAGT1, FAS, FASLG, CASP10, ITK, FADD, CTLA4
Specificity
10 %
Genes
20 %
Hereditary Leukemia/Lymphoma Panel.

By Baylor Miraca Genetics Laboratories in United States.

BRCA2, RUNX1, TP53, PTPN11, CBL, ATM, PALB2, BRIP1, GATA2, PAX5, SBDS, CEBPA, PRF1
Specificity
8 %
Genes
20 %
Comprehensive Hereditary Cancer Panel.

By Baylor Miraca Genetics Laboratories in United States.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RUNX1, TP53, WT1, SDHAF2, RET, SDHC, FH, SDHB, TMEM127 , (...)

View the complete list with 41 more genes
Specificity
2 %
Genes
20 %
Bone Marrow Failure.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

BRCA2, RPL35A, FANCC, RPS19, TINF2, NBN, PALB2, BRIP1, SBDS, PRF1, RAD51C, MPL, GATA1, RPS26, RPS10, RPL11, RPL5, RPS24, FANCB, DKC1 , (...)

View the complete list with 23 more genes
Specificity
3 %
Genes
20 %
PRF1 Sequencing.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

PRF1
Specificity
100 %
Genes
20 %
Hemophagocytic Lymphohistiocytosis Panel by next generation sequencing (NGS).

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

AP3B1, PRF1, SLC7A7, MAGT1, BLOC1S6, LYST, SH2D1A, RAB27A, UNC13D, STX11, XIAP, STXBP2, ITK, CD27
Specificity
8 %
Genes
20 %
Hemophagocytic Lymphohistiocytosis Deletion/Duplication Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

AP3B1, PRF1, SLC7A7, MAGT1, BLOC1S6, LYST, SH2D1A, RAB27A, UNC13D, STX11, XIAP, STXBP2, ITK, CD27
Specificity
8 %
Genes
20 %
PRF1 Deletion/duplication analysis.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

PRF1
Specificity
100 %
Genes
20 %
Ataxia Exome Panel.

By Genetic Services Laboratory University of Chicago in United States.

FMR1, TTR, UBE3A, AARS2, ABHD12, PC, UQCRQ, UQCRB, HLCS, BTD, ATP7B, ATPAF2, AUH, BCKDHA, BCKDHB, BCS1L, TWNK, C12orf65, ADSL, PRKCG , (...)

View the complete list with 460 more genes
Specificity
1 %
Genes
20 %
PRF1.

By Institute for Human Genetics University Clinic Freiburg in Germany.

PRF1
Specificity
100 %
Genes
20 %
PRF1. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

PRF1
Specificity
100 %
Genes
20 %
Hemophagocytic lymphohistiocytosis and reticuloendotheliosis with eosinophilia, familial (NGS panel for 7 genes).

By CGC Genetics in Portugal.

PRF1, DCLRE1C, RAG2, RAG1, UNC13D, STX11, STXBP2
Specificity
15 %
Genes
20 %
Hemophagocytic lymphohistiocytosis, familial (sequence analysis of PRF1 gene).

By CGC Genetics in Portugal.

PRF1
Specificity
100 %
Genes
20 %
OncoRisk Plus (NGS panel for 89 genes).

By CGC Genetics in Portugal.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, WT1, RB1, SDHAF2, RET, SDHC, FH , (...)

View the complete list with 69 more genes
Specificity
2 %
Genes
20 %
Familial Hemophagocytic Lymphohistiocytosis (FHL) Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

AP3B1, ADA, IL2RG, PNP, PRF1, SLC7A7, WAS, BTK, NLRP3, MVK, MAGT1, BLOC1S6, LYST, MEFV, SH2D1A, RAB27A, UNC13D, STX11, XIAP, STXBP2 , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
20 %
Familial Hemophagocytic Lymphohistiocytosis-Type 2 (FHL2) via PRF1 Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

PRF1
Specificity
100 %
Genes
20 %
Hereditary Cancer Syndromes - panels.

By MGZ Medical Genetics Center in Germany.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, HNF1A, WT1, RB1, SDHAF2, RET, SDHC , (...)

View the complete list with 80 more genes
Specificity
1 %
Genes
20 %
Familial Hemophagocytic Lymphohistiocytosis Panel.

By FirmaLab in United States.

PRF1, RAB27A, UNC13D, STX11, STXBP2
Specificity
20 %
Genes
20 %
PRF1.

By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.

PRF1
Specificity
100 %
Genes
20 %
HLH/immunedisregulation panel.

By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.

AP3B1, PRF1, LYST, SH2D1A, RAB27A, UNC13D, STX11, XIAP, STXBP2
Specificity
12 %
Genes
20 %
Hemophagocytic Lymphohistiocytosis panel.

By Centogene AG - the Rare Disease Company in Germany.

PRF1, UNC13D, STX11, STXBP2
Specificity
25 %
Genes
20 %
Hemophagocytic lymphohistiocytosis, familial type 1.

By Centogene AG - the Rare Disease Company in Germany.

PRF1
Specificity
100 %
Genes
20 %
Aplastic anemia.

By Centogene AG - the Rare Disease Company in Germany.

PRF1
Specificity
100 %
Genes
20 %
Leukodystrophy / Leukencephalopathy and differential diagnoses Panel.

By CeGaT GmbH in Germany.

AARS2, PC, TYROBP, ATP7A, ATP7B, AUH, BCS1L, C12orf65, MMACHC, HSD17B4, PSAP, GLB1, OCRL, POLG, NDUFS4, HSPD1, FOXRED1, NDUFAF2, NDUFA12, NDUFA9 , (...)

View the complete list with 155 more genes
Specificity
1 %
Genes
20 %
Single gene testing PRF1.

By CeGaT GmbH in Germany.

PRF1
Specificity
100 %
Genes
20 %
Bone marrow failure syndromes Panel.

By CeGaT GmbH in Germany.

BRCA2, FANCC, TINF2, MRE11, NBN, PALB2, BRIP1, SBDS, PRF1, RAD51C, RTEL1, WAS, FANCB, DKC1, LYST, TERC, TERT, CSF2RA, CTC1, WRAP53 , (...)

View the complete list with 17 more genes
Specificity
3 %
Genes
20 %
Cancer Predisposition.

By Asper Biogene Asper Biogene LLC in Estonia.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, HNF1A, WT1, RB1, SDHAF2, RET, SDHC, FH , (...)

View the complete list with 69 more genes
Specificity
2 %
Genes
20 %
Familial hemophagocytic lymphohistiocytosis, PRF1 sequencing.

By Molecular Diagnostics Laboratory Seoul National University Hospital in South Korea.

PRF1
Specificity
100 %
Genes
20 %
Hemophagocytic Lymphohistiocytosis 2.

By Praxis fuer Humangenetik Wien in Austria.

PRF1
Specificity
100 %
Genes
20 %
Hemophagocytic Lymphohistiocytosis 2.

By MedGene in Slovakia.

PRF1
Specificity
100 %
Genes
20 %
Invitae Hereditary Hemophagocytic Lymphohistiocytosis (HLH) Disorders Panel.

By Invitae in United States.

AP3B1, ADA, IL2RG, PNP, PRF1, SLC7A7, WAS, BTK, MVK, MAGT1, BLOC1S6, LYST, SH2D1A, RAB27A, UNC13D, STX11, XIAP, STXBP2, ITK, CD27 , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
20 %
Hemophagocytic Lymphohistiocytosis, Familial: PRF1 gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

PRF1
Specificity
100 %
Genes
20 %
Hemophagocytic lymphohistiocytosis, familial.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

PRF1, SH2D1A, RAB27A, UNC13D, STX11, STXBP2
Specificity
17 %
Genes
20 %
Hemophagocytic Lymphohistiocytosis: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

AP3B1, GATA2, PRF1, SLC7A7, MAGT1, BLOC1S6, LYST, SH2D1A, RAB27A, UNC13D, STX11, XIAP, STXBP2, ITK, CD27, NLRC4
Specificity
7 %
Genes
20 %
Familial Hemophagocytic Lymphohistiocytosis NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

PRF1, RAB27A, UNC13D, STX11, STXBP2
Specificity
20 %
Genes
20 %
PRF1.

By Fulgent Genetics Fulgent Genetics in United States.

PRF1
Specificity
100 %
Genes
20 %
Hereditary Pediatric Cancer Panel.

By Blueprint Genetics in Finland.

VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, PTEN, RECQL4, RUNX1, TP53, WT1, SDHAF2, RET, SDHC, RAF1, FH, SDHB, TMEM127, MEN1 , (...)

View the complete list with 51 more genes
Specificity
2 %
Genes
20 %
Comprehensive Hereditary Cancer Panel.

By Blueprint Genetics in Finland.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, HNF1A, WT1, SDHAF2, RET, SDHC, RAF1 , (...)

View the complete list with 126 more genes
Specificity
1 %
Genes
20 %
Hemophagocytic Lymphohistiocytosis Panel.

By Blueprint Genetics in Finland.

RECQL4, PRF1, MAGT1, LYST, SH2D1A, MYO5A, RAB27A, UNC13D, FAS, STX11, XIAP, FASLG, STXBP2, ITK, FADD
Specificity
7 %
Genes
20 %
Comprehensive Hematology Panel.

By Blueprint Genetics in Finland.

BRCA1, BRCA2, F2, F5, HFE, EPCAM, MSH2, PMS2, MSH6, MLH1, RECQL4, RUNX1, TP53, YARS2, PC, HBB, TYRP1, OCA2, AMN, SLC45A2 , (...)

View the complete list with 219 more genes
Specificity
1 %
Genes
20 %
Bone Marrow Failure Syndrome Panel.

By Blueprint Genetics in Finland.

BRCA1, BRCA2, EPCAM, MSH2, PMS2, MSH6, MLH1, RECQL4, RUNX1, TP53, SLC37A4, DTNBP1, HPS1, BLOC1S3, HPS6, HPS5, HPS4, HPS3, RPL35A, HAX1 , (...)

View the complete list with 102 more genes
Specificity
1 %
Genes
20 %
Amyotrophic Lateral Sclerosis Panel.

By Blueprint Genetics in Finland.

OPTN, HSPD1, VCP, REEP1, GRN, SQSTM1, HEXA, GBE1, SOD1, PRF1, FIG4, ATL1, SPG11, SPAST, KIF5A, BSCL2, WASHC5, SPART, ALS2, FUS , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
20 %
Familial hemophagocytic lymphohistiocytosis 2.

By Bioarray in Spain.

PRF1
Specificity
100 %
Genes
20 %
FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS.

By Laboratorio de Genetica Clinica SL in Spain.

PRF1, UNC13D, STX11, STXBP2
Specificity
25 %
Genes
20 %
Familial Hemophagocytic Lymphohistiocytosis Type 2 , Sequencing PRF1 Gene.

By Reference Laboratory Genetics in Spain.

PRF1
Specificity
100 %
Genes
20 %
Familial Hemophagocytic Lymphohistiocytosis , Panel Massive Sequencing (NGS) 16 Genes.

By Reference Laboratory Genetics in Spain.

AP3B1, PRF1, SLC7A7, MAGT1, BLOC1S6, LYST, SH2D1A, RAB27A, RAG2, RAG1, UNC13D, STX11, XIAP, STXBP2, ITK, CD27
Specificity
7 %
Genes
20 %
Oncology Genetic Panel , Panel Massive Sequencing (NGS) 90 Genes.

By Reference Laboratory Genetics in Spain.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, HNF1A, WT1, RB1, SDHAF2, RET, SDHC , (...)

View the complete list with 70 more genes
Specificity
2 %
Genes
20 %
Idiopathic Aplastic Anemia , Panel Massive Sequencing (NGS) 6 Genes.

By Reference Laboratory Genetics in Spain.

NBN, SBDS, PRF1, TERC, TERT, IFNG
Specificity
17 %
Genes
20 %
Familial Hemophagocytic Lymphohistiocytosis: gene sequencing panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

PRF1, UNC13D, STX11, STXBP2
Specificity
25 %
Genes
20 %

Alternate names

Lymphoma, Non-hodgkin, Familial Is also known as non-hodgkin lymphoma;nhl;nhl.



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