Pancreatic Agenesis 1; Pagen1

Description

Partial agenesis of the pancreas is characterized by the congenital absence of a critical mass of pancreatic tissue.

Clinical Features

Top most frequent phenotypes and symptoms related to Pancreatic Agenesis 1; Pagen1

  • Growth delay
  • Failure to thrive
  • Intrauterine growth retardation
  • Diabetes mellitus
  • Malabsorption
  • Type II diabetes mellitus
  • Recurrent skin infections
  • Increased body weight
  • Hyperglycemia
  • Glucose intolerance
And another 5 symptoms. If you need more information about this disease we can help you.
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Incidence and onset information

Not enough data available about incidence and published cases.


Mendelian

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Pancreatic Agenesis 1; Pagen1 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Maturity-Onset Diabetes of the Young.

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

HNF1A, NEUROD1, HNF1B, WFS1, GCK, CISD2, ABCC8, KCNJ11, INS, PDX1, HNF4A, FOXP3, CP, IER3IP1, SLC2A2, AKT2, RFX6, PAX4, KLF11, BLK , (...)

View the complete list with 5 more genes
Specificity
8 %
Genes
100 %
Neonatal Diabetes Mellitus and Maturity-Onset Diabetes of the Young Deletion/Duplication Panel.

By Genetic Services Laboratory University of Chicago in United States.

NEUROD1, WFS1, GCK, GLUD1, CISD2, STAT3, AIRE, CDKN1C, ABCC8, CEL, KCNJ11, INS, PDX1, FOXP3, CP, GATA4, IER3IP1, PCBD1, HADH, SLC2A2 , (...)

View the complete list with 21 more genes
Specificity
5 %
Genes
100 %
Neonatal Diabetes Mellitus and Maturity-Onset Diabetes of the Young Panel.

By Genetic Services Laboratory University of Chicago in United States.

NEUROD1, WFS1, GCK, GLUD1, CISD2, STAT3, AIRE, CDKN1C, ABCC8, CEL, KCNJ11, INS, PDX1, FOXP3, CP, GATA4, IER3IP1, PCBD1, HADH, SLC2A2 , (...)

View the complete list with 21 more genes
Specificity
5 %
Genes
100 %
PTF1A deletion/duplication analysis.

By Genetic Services Laboratory University of Chicago in United States.

PTF1A
Specificity
100 %
Genes
50 %
PTF1A sequencing.

By Genetic Services Laboratory University of Chicago in United States.

PTF1A
Specificity
100 %
Genes
50 %
Pancreatic agenesis 2 (sequence analysis of PTF1A gene).

By CGC Genetics in Portugal.

PTF1A
Specificity
100 %
Genes
50 %
Diabetes mellitus permanent neonatal (NGS panel for 13 genes).

By CGC Genetics in Portugal.

PAX6, HNF1B, GCK, ABCC8, KCNJ11, INS, PDX1, SLC19A2, IER3IP1, RFX6, GLIS3, PTF1A, GATA6
Specificity
16 %
Genes
100 %
Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis.

By Exeter Molecular Genetics Laboratory in United Kingdom.

PTF1A
Specificity
100 %
Genes
50 %
KCNJ11-Related Permanent Neonatal Diabetes Mellitus.

By Exeter Molecular Genetics Laboratory in United Kingdom.

PTF1A
Specificity
100 %
Genes
50 %
AllNeuro panel.

By Centogene AG - the Rare Disease Company in Germany.

F2, F5, FMR1, HTT, HFE, MTHFR, TTR, UBE3A, VHL, PTEN, AARS2, ABHD12, ACACA, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1 , (...)

View the complete list with 1185 more genes
Specificity
1 %
Genes
50 %
CentoICU platinum plus.

By Centogene AG - the Rare Disease Company in Germany.

BRCA2, F2, F5, MTHFR, UBE3A, MCCC1, MCCC2, AARS2, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1, ALDOA, ALDOB, FBP1, PC, GYS2 , (...)

View the complete list with 494 more genes
Specificity
1 %
Genes
100 %
CentoICU platinum.

By Centogene AG - the Rare Disease Company in Germany.

BRCA2, F2, F5, MTHFR, UBE3A, MCCC1, MCCC2, AARS2, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1, ALDOA, ALDOB, FBP1, PC, GYS2 , (...)

View the complete list with 494 more genes
Specificity
1 %
Genes
100 %
Pancreatic and cerebellar agenesis.

By Centogene AG - the Rare Disease Company in Germany.

PTF1A
Specificity
100 %
Genes
50 %
Pancreatic agenesis type 2.

By Centogene AG - the Rare Disease Company in Germany.

PTF1A
Specificity
100 %
Genes
50 %
Spinocerebellar Ataxia.

By Asper Biogene Asper Biogene LLC in Estonia.

ABHD12, TWNK, PRKCG, WFS1, ELOVL4, AFG3L2, ACO2, COQ8A, DARS2, POLG2, FLVCR1, ABCB7, SLC9A6, PHYH, FXN, CYP27A1, APTX, TPP1, WWOX, NPC1 , (...)

View the complete list with 45 more genes
Specificity
2 %
Genes
50 %
Cardiovascular Diseases_General Panel.

By Health in Code in Spain.

HFE, TTR, AARS2, ACAD9, AGL, ACADVL, ATP5F1E, ATP7A, ATPAF2, B4GALT7, GAA, HNF1A, NEUROD1, PPARG, COL1A1, COL1A2, COL3A1, ELAC2, PSEN1, HNF1B , (...)

View the complete list with 360 more genes
Specificity
1 %
Genes
100 %
Maturity-onset diabetes of the young MODY.

By Health in Code in Spain.

HNF1A, NEUROD1, HNF1B, WFS1, GCK, CEL, KCNJ11, INS, PDX1, HNF4A, FOXP3, IER3IP1, SLC2A2, RFX6, PAX4, KLF11, BLK, GLIS3, NEUROG3, PTF1A , (...)

View the complete list with 3 more genes
Specificity
9 %
Genes
100 %
Dyslipidemias / Early atherosclerosis.

By Health in Code in Spain.

HNF1A, NEUROD1, PPARG, HNF1B, CPT2, WFS1, PCDH15, GCK, GPD1, CAVIN1, PNPLA2, MEF2A, COQ2, PYGM, LDLR, LEP, LIPA, MTTP, LMNA, APOE , (...)

View the complete list with 64 more genes
Specificity
3 %
Genes
100 %
Diabetes mellitus, neonatal permanent.

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

NEUROD1, PAX6, HNF1B, WFS1, GCK, ABCC8, KCNJ11, INS, PDX1, SLC19A2, FOXP3, RFX6, GLIS3, NEUROG3, PTF1A, GATA6, EIF2AK3
Specificity
12 %
Genes
100 %
Endocrine Disorders: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

HNF1A, NEUROD1, PPARG, HNF1B, WFS1, GCK, CAVIN1, CISD2, CYP17A1, CHD7, ABCC8, LMNA, NR0B1, GNRH1, FGFR1, LHCGR, KCNJ11, TACR3, KISS1R, GNRHR , (...)

View the complete list with 37 more genes
Specificity
4 %
Genes
100 %
Endocrine Disorders: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

HNF1A, NEUROD1, PPARG, HNF1B, WFS1, GCK, CAVIN1, CISD2, CYP17A1, CHD7, ABCC8, LMNA, NR0B1, GNRH1, FGFR1, LHCGR, KCNJ11, TACR3, KISS1R, GNRHR , (...)

View the complete list with 37 more genes
Specificity
4 %
Genes
100 %
Diabetes-Obesity NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

HNF1A, NEUROD1, HNF1B, WFS1, ARL6, MKKS, CEP290, TTC8, TRIM32, GCK, BBS7, BBS5, BBS12, MKS1, BBS9, BBS10, BBS4, BBS1, BBS2, ALMS1 , (...)

View the complete list with 24 more genes
Specificity
5 %
Genes
100 %
MODY Neonatal Diabetes NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

HNF1A, NEUROD1, HNF1B, WFS1, GCK, GLUD1, CISD2, ABCC8, CEL, KCNJ11, INS, PDX1, HNF4A, FOXP3, CP, IER3IP1, HADH, SLC2A2, AKT2, RFX6 , (...)

View the complete list with 10 more genes
Specificity
7 %
Genes
100 %
PTF1A.

By Fulgent Genetics Fulgent Genetics in United States.

PTF1A
Specificity
100 %
Genes
50 %
Comprehensive Monogenic Diabetes Panel.

By Blueprint Genetics in Finland.

HNF1A, NEUROD1, PPARG, HNF1B, SLC16A1, WFS1, GCK, UCP2, GLUD1, ABCC8, KCNJ11, INS, PDX1, HNF4A, FOXP3, HADH, SLC2A2, RFX6, PAX4, KLF11 , (...)

View the complete list with 8 more genes
Specificity
8 %
Genes
100 %
Comprehensive Metabolism Panel.

By Blueprint Genetics in Finland.

HFE, MTHFR, MCCC1, MCCC2, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1, ALDOA, ALDOB, FBP1, PC, GYS2, ARG1, HLCS, BTD, ATP7B , (...)

View the complete list with 414 more genes
Specificity
1 %
Genes
100 %
Gastrointestinal Atresia Panel.

By Blueprint Genetics in Finland.

SOX2, FANCC, CHD7, DHCR7, MID1, FANCB, GLI3, EFTUD2, MYCN, RFX6, PTF1A, TTC7A, CLMP
Specificity
8 %
Genes
50 %
Hypoglycemia, Hyperinsulinism and Ketone Metabolism Panel.

By Blueprint Genetics in Finland.

AGL, ACAT1, ALDOA, ALDOB, FBP1, PC, GYS2, GAA, HNF1A, SLC37A4, SLC16A1, GCK, ACSF3, PHKA2, HMGCL, PYGL, G6PC, PHKG2, PGM1, LDHA , (...)

View the complete list with 30 more genes
Specificity
4 %
Genes
100 %
DIABETES MODY & NEONATAL DIABETES : NGS PANEL.

By Laboratorio de Genetica Clinica SL in Spain.

HNF1A, NEUROD1, HNF1B, GCK, GLUD1, ABCC8, KCNJ11, INS, PDX1, HNF4A, FOXP3, IER3IP1, SLC2A2, RFX6, PAX4, KLF11, BLK, GLIS3, PTF1A, EIF2AK3 , (...)

View the complete list with 2 more genes
Specificity
10 %
Genes
100 %
Pancreatic Agenesis Type 2 , Sequencing PTF1A Gene.

By Reference Laboratory Genetics in Spain.

PTF1A
Specificity
100 %
Genes
50 %
Permanent Neonatal Diabetes Mellitus , Panel Massive Sequencing (NGS) 16 Genes.

By Reference Laboratory Genetics in Spain.

NEUROD1, HNF1B, WFS1, GCK, ABCC8, KCNJ11, INS, PDX1, SLC19A2, FOXP3, RFX6, GLIS3, NEUROG3, PTF1A, GATA6, EIF2AK3
Specificity
13 %
Genes
100 %
Neonatal Diabetes Mellitus Evaluation.

By Athena Diagnostics Inc in United States.

GCK, ABCC8, KCNJ11, INS, PDX1
Specificity
20 %
Genes
50 %
Monogenic Diabetes (MODY) Five Gene Evaluation (GCK,HNF1A,HNF1B,HNF4A,IPF1).

By Athena Diagnostics Inc in United States.

HNF1A, HNF1B, GCK, PDX1, HNF4A
Specificity
20 %
Genes
50 %
IPF1 (MODY4) DNA Sequencing Test.

By Athena Diagnostics Inc in United States.

PDX1
Specificity
100 %
Genes
50 %
IPF1 (NDM) DNA Sequencing Test.

By Athena Diagnostics Inc in United States.

PDX1
Specificity
100 %
Genes
50 %
Maturity-onset Diabetes of the Young Panel.

By Genetic Diagnostic Laboratory University of Pennsylvania School of Medicine in United States.

HNF1A, NEUROD1, HNF1B, GCK, ABCC8, CEL, KCNJ11, INS, PDX1, HNF4A, AKT2, PAX4, KLF11, BLK, INSR
Specificity
7 %
Genes
50 %
PDX1 Deletion/duplication analysis.

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

PDX1
Specificity
100 %
Genes
50 %
PDX1 Sequencing.

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

PDX1
Specificity
100 %
Genes
50 %
MODY Deletion/Duplication Panel.

By Genetic Services Laboratory University of Chicago in United States.

HNF1A, NEUROD1, HNF1B, GCK, ABCC8, CEL, KCNJ11, INS, PDX1, HNF4A, PAX4, KLF11, BLK, APPL1
Specificity
8 %
Genes
50 %
Comprehensive Neonatal Diabetes Mutation Analysis.

By Genetic Services Laboratory University of Chicago in United States.

GCK, ABCC8, KCNJ11, INS, PDX1, FOXP3, GATA4, GATA6, EIF2AK3, NKX2-2, MNX1, ZFP57, PLAGL1, HYMAI
Specificity
8 %
Genes
50 %
PDX1 deletion/duplication analysis.

By Genetic Services Laboratory University of Chicago in United States.

PDX1
Specificity
100 %
Genes
50 %
PDX1 sequencing.

By Genetic Services Laboratory University of Chicago in United States.

PDX1
Specificity
100 %
Genes
50 %
MODY Panel.

By Genetic Services Laboratory University of Chicago in United States.

HNF1A, NEUROD1, HNF1B, GCK, ABCC8, CEL, KCNJ11, INS, PDX1, HNF4A, PAX4, KLF11, BLK, APPL1
Specificity
8 %
Genes
50 %
Neonatal Diabetes Mellitus Deletion/Duplication Analysis.

By Genetic Services Laboratory University of Chicago in United States.

GCK, ABCC8, KCNJ11, INS, PDX1, FOXP3, EIF2AK3, ZFP57
Specificity
13 %
Genes
50 %
Neonatal Diabetes Mellitus Sequencing Panel.

By Genetic Services Laboratory University of Chicago in United States.

GCK, ABCC8, KCNJ11, INS, PDX1, FOXP3, GATA4, GATA6, EIF2AK3, NKX2-2, MNX1, ZFP57
Specificity
9 %
Genes
50 %
MODY Panel.

By Ambry Genetics in United States.

HNF1A, HNF1B, GCK, PDX1, HNF4A
Specificity
20 %
Genes
50 %
MODY 4 (sequence analysis of PDX1 gene).

By CGC Genetics in Portugal.

PDX1
Specificity
100 %
Genes
50 %
Permanent neonatal diabetes mellitus (deletion/duplication analysis of PDX1 gene).

By CGC Genetics in Portugal.

PDX1
Specificity
100 %
Genes
50 %
Pancreatic agenesis (sequence analysis of PDX1 gene).

By CGC Genetics in Portugal.

PDX1
Specificity
100 %
Genes
50 %
MODY (NGS panel for 13 genes).

By CGC Genetics in Portugal.

HNF1A, NEUROD1, HNF1B, GCK, ABCC8, CEL, KCNJ11, INS, PDX1, HNF4A, PAX4, KLF11, BLK
Specificity
8 %
Genes
50 %
Maturity-onset diabetes of the young, type 4.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

PDX1
Specificity
100 %
Genes
50 %
Maturity Onset Diabetes of the Young (Types 1 to 10).

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

HNF1A, NEUROD1, HNF1B, GCK, CEL, INS, PDX1, HNF4A, PAX4, KLF11, BLK
Specificity
10 %
Genes
50 %
Neonatal Diabetes Mellitus.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

GCK, ABCC8, KCNJ11, INS, PDX1, ZFP57
Specificity
17 %
Genes
50 %
MODY4 Diabetes.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

PDX1
Specificity
100 %
Genes
50 %
Maturity-Onset Diabetes of the Young Subtype PDX1.

By Exeter Molecular Genetics Laboratory in United Kingdom.

PDX1
Specificity
100 %
Genes
50 %
Maturity Onset Diabetes of the Young (MODY) Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

HNF1A, NEUROD1, HNF1B, GCK, ABCC8, KCNJ11, INS, PDX1, HNF4A, PAX4, KLF11, BLK, APPL1
Specificity
8 %
Genes
50 %
Maturity Onset Diabetes of the Young (MODY) via the PDX1 Gene.

By PreventionGenetics PreventionGenetics in United States.

PDX1
Specificity
100 %
Genes
50 %
PDX1.

By Department of Clinical Genetics Odense University Hospital in Denmark.

PDX1
Specificity
100 %
Genes
50 %
Nephrology Endocrinology and Electrolytes - panels.

By MGZ Medical Genetics Center in Germany.

VHL, ALPL, HNF1A, NEUROD1, EYA1, WT1, HNF1B, RET, OCRL, GCK, COQ9, PDSS2, COQ6, CYP24A1, COQ2, AGXT, SLC3A1, LMX1B, PAX2, GLA , (...)

View the complete list with 97 more genes
Specificity
1 %
Genes
50 %
Maturity Onset Diabetes of the Young.

By Synlab MVZ Humane Genetik München Synlab MVZ Humane Genetik München in Germany.

HNF1A, NEUROD1, HNF1B, GCK, PDX1, HNF4A, KLF11
Specificity
15 %
Genes
50 %
Comprehensive mitochondrial disorders panel.

By Centogene AG - the Rare Disease Company in Germany.

MCCC1, MCCC2, ACAD9, ACADM, ACADS, ACADVL, ACAT1, PC, UQCRB, HLCS, ATP5F1E, ATP7B, ATPAF2, AUH, BCKDHA, BCKDHB, BCS1L, TWNK, STAR, MTRR , (...)

View the complete list with 160 more genes
Specificity
1 %
Genes
50 %
MODY panel.

By Centogene AG - the Rare Disease Company in Germany.

HNF1A, NEUROD1, HNF1B, GCK, ABCC8, CEL, INS, PDX1, HNF4A, RFX6, PAX4, KLF11, BLK, NKX2-2, ZFP57
Specificity
7 %
Genes
50 %
Maturity-onset diabetes of the young type 4.

By Centogene AG - the Rare Disease Company in Germany.

PDX1
Specificity
100 %
Genes
50 %
ABCC8-Related Hyperinsulinism.

By bio.logis Center for Human Genetics Diagnosticum in Germany.

GCK, GLUD1, ABCC8, KCNJ11, PDX1, HNF4A, HADH
Specificity
15 %
Genes
50 %
Maturity onset diabetes mellitus in young.

By bio.logis Center for Human Genetics Diagnosticum in Germany.

HNF1A, NEUROD1, HNF1B, GCK, CEL, INS, PDX1, HNF4A, PAX4, KLF11, BLK
Specificity
10 %
Genes
50 %
Maturity-Onset Diabetes of the Young Type 4 (PDX1, MODY4).

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

PDX1
Specificity
100 %
Genes
50 %
Mitochondrial Diseases (mtDNA and 133 nuclear genes).

By Asper Biogene Asper Biogene LLC in Estonia.

AARS2, ACAD9, ACADL, ACADM, ACADS, ACADVL, YARS2, FBP1, PC, GYS2, UQCRQ, UQCRB, HLCS, ATP5F1E, ATPAF2, AUH, BCS1L, TWNK, C12orf65, SLC37A4 , (...)

View the complete list with 112 more genes
Specificity
1 %
Genes
50 %
Maturity Onset Diabetes of the Young (MODY).

By Asper Biogene Asper Biogene LLC in Estonia.

HNF1A, NEUROD1, HNF1B, GCK, ABCC8, CEL, KCNJ11, INS, PDX1, HNF4A, RFX6, PAX4, KLF11, BLK, ZFP57
Specificity
7 %
Genes
50 %
MODY 04.

By Praxis fuer Humangenetik Wien in Austria.

PDX1
Specificity
100 %
Genes
50 %
Pancreatic agenesis.

By Praxis fuer Humangenetik Wien in Austria.

PDX1
Specificity
100 %
Genes
50 %
MODY 04.

By MedGene in Slovakia.

PDX1
Specificity
100 %
Genes
50 %
Pancreatic agenesis.

By MedGene in Slovakia.

PDX1
Specificity
100 %
Genes
50 %
MODY type 4: IPF1 gene sequence analysis.

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

PDX1
Specificity
100 %
Genes
50 %
DIABETES (MODY).

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

HNF1A, NEUROD1, HNF1B, GCK, KCNJ11, PDX1, HNF4A, SLC2A2, PAX4, KLF11, BLK
Specificity
10 %
Genes
50 %
Maturity Onset Diabetes of the Young (MODY): Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

HNF1A, GCK, PDX1, HNF4A
Specificity
25 %
Genes
50 %
Hyperinsulinism NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

SLC16A1, GCK, UCP2, GLUD1, ABCC8, KCNJ11, INS, PDX1, HNF4A, HADH, INSR
Specificity
10 %
Genes
50 %
Nuclear-Mito NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

HTT, UBE3A, MUTYH, TP53, MCCC1, MCCC2, AARS2, ACACA, ACAD9, ACADL, ACADM, ACADS, ACADVL, ACAT1, YARS2, FBP1, PC, GYS2, UQCRQ, UQCRB , (...)

View the complete list with 484 more genes
Specificity
1 %
Genes
50 %
PDX1.

By Fulgent Genetics Fulgent Genetics in United States.

PDX1
Specificity
100 %
Genes
50 %
MODY Panel.

By Blueprint Genetics in Finland.

HNF1A, NEUROD1, HNF1B, GCK, ABCC8, KCNJ11, INS, PDX1, HNF4A, RFX6, PAX4, KLF11, BLK
Specificity
8 %
Genes
50 %
Maturity-Onset Diabetes of the Young NGS and Deletion/Duplication Panel.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

HNF1A, NEUROD1, HNF1B, GCK, ABCC8, CEL, KCNJ11, INS, PDX1, HNF4A, PAX4, KLF11, BLK
Specificity
8 %
Genes
50 %
PDX1 Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

PDX1
Specificity
100 %
Genes
50 %
Monogenic Diabetes NGS and Deletion/Duplication Panel.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

HNF1A, NEUROD1, PPARG, HNF1B, SLC16A1, WFS1, GCK, UCP2, GLUD1, ABCC8, CEL, KCNJ11, INS, PDX1, HNF4A, FOXP3, HADH, SLC2A2, PAX4, KLF11 , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
50 %
MATURITY-ONSET DIABETES OF THE YOUNG (MODY) TYPE 4.

By Laboratorio de Genetica Clinica SL in Spain.

PDX1
Specificity
100 %
Genes
50 %
MODY panel.

By LifeLabs Genetics in Canada.

HNF1A, NEUROD1, HNF1B, GCK, ABCC8, CEL, INS, PDX1, HNF4A, RFX6, PAX4, KLF11, BLK, NKX2-2, ZFP57
Specificity
7 %
Genes
50 %
Diabetes MODY Type 4, Sequencing IPF1 Gene.

By Reference Laboratory Genetics in Spain.

PDX1
Specificity
100 %
Genes
50 %
Pancreatic Agenesis , Sequencing PDX1 Gene.

By Reference Laboratory Genetics in Spain.

PDX1
Specificity
100 %
Genes
50 %
Diabetes MODY Types 4-10 , Deletions-Duplications (MLPA) PDX1, NEUROD1, KLF11, CEL, PAX4, INS Genes.

By Reference Laboratory Genetics in Spain.

NEUROD1, CEL, INS, PDX1, PAX4, KLF11
Specificity
17 %
Genes
50 %
Diabetes MODY, Panel Massive Sequencing (NGS) 11 Genes.

By Reference Laboratory Genetics in Spain.

HNF1A, NEUROD1, HNF1B, GCK, KCNJ11, PDX1, HNF4A, SLC2A2, PAX4, KLF11, BLK
Specificity
10 %
Genes
50 %
Maturity-onset diabetes of the young, type 4.

By Labor Dr. Wisplinghoff in Germany.

PDX1
Specificity
100 %
Genes
50 %
Permanent Neonatal Diabetes Mellitus: gene sequencing panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

GCK, ABCC8, KCNJ11, INS, PDX1
Specificity
20 %
Genes
50 %

Alternate names

Pancreatic Agenesis 1; Pagen1 Is also known as pagen, pancreatic hypoplasia, congenital;congenital pancreatic agenesis; partial agenesis of the pancreas.


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