Biliary Cirrhosis, Primary, 1; Pbc1

Description

Primary biliary cirrhosis (PBC) is a chronic, progressive cholestatic liver disease that usually affects middle-aged women and eventually leads to liver failure (summary by Kaplan, 1996). Genetic Heterogeneity of Primary Biliary CirrhosisPrimary biliary cirrhosis-1 (PBC1) is significantly associated with SNPs at the IL12A locus (OMIM ) on chromosome 3p12-q13.2.Significant association of PBC has also been shown with SNPs at the HLA-DQB1 locus (OMIM ) on chromosome 6p21.3 (PBC2 ), at the IL12RB2 locus (OMIM ) on chromosome 1p31.2 (PBC3 ), at the IRF5 (OMIM )-TNPO3 (OMIM ) locus on chromosome 7q32 (PBC4 ), and at the ZPBP2 locus (OMIM ) on chromosome 17q12-q21 (PBC5 ).See also Reynolds syndrome (OMIM ), in which primary biliary cirrhosis is a feature.

Clinical Features

Top most frequent phenotypes and symptoms related to Biliary Cirrhosis, Primary, 1; Pbc1

  • Fatigue
  • Osteoporosis
  • Jaundice
  • Pruritus
  • Autoimmunity
  • Cirrhosis
  • Sleep disturbance
  • Hepatic failure
  • Ascites
  • Abdominal distention
And another 23 symptoms. If you need more information about this disease we can help you.
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Incidence and onset information

— Based on the latest data available Biliary Cirrhosis, Primary, 1; Pbc1 have a estimated prevalence of 21.05 per 100k in Europe.


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Biliary Cirrhosis, Primary, 1; Pbc1 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
TNFSF15.

By Fulgent Genetics Fulgent Genetics in United States.

TNFSF15
Specificity
100 %
Genes
13 %
POU2AF1.

By Fulgent Genetics Fulgent Genetics in United States.

POU2AF1
Specificity
100 %
Genes
13 %
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
13 %
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
50 %
Muscular Dystrophies NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

TRIM32, CAVIN1, DPM3, DMD, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, ANO5, MYOT, FHL1, SYNE1 , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
13 %
MMEL1.

By Fulgent Genetics Fulgent Genetics in United States.

MMEL1
Specificity
100 %
Genes
13 %
Neuromuscular Disorders Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

ATP7A, TWNK, GAA, GNE, TRIM32, POLG, SLC25A4, GARS, RRM2B, CRYAB, VCP, AGK, CAVIN1, DPM3, SUCLA2, PNPLA2, REEP1, POLG2, TK2, DPM1 , (...)

View the complete list with 124 more genes
Specificity
1 %
Genes
13 %
Neuromuscular Disorders Sequencing Panel.

By Genetic Services Laboratory University of Chicago in United States.

GAA, GNE, TRIM32, CRYAB, VCP, DPM3, DPM1, ALG2, CHAT, PYGM, GBE1, DPAGT1, DMD, HRAS, CHRNE, DOK7, FKTN, NEB, SGCA, SGCB , (...)

View the complete list with 91 more genes
Specificity
1 %
Genes
13 %
Limb-Girdle Muscular Dystrophy Sequencing Panel.

By Genetic Services Laboratory University of Chicago in United States.

GAA, TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, TRAPPC11, DNAJB6, DAG1 , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
13 %
Limb-Girdle Muscular Dystrophy Deletion/Duplication Panel.

By Genetic Services Laboratory University of Chicago in United States.

GAA, TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, TRAPPC11, DNAJB6, DAG1 , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
13 %
Limb-girdle muscular dystrophies (NGS panel for 26 genes).

By CGC Genetics in Portugal.

TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, ANO5, MYOT, TRAPPC11, DNAJB6, DAG1, PLEC, POMT2 , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
13 %
Muscular dystrophy, limb-girdle (sequence analysis of TNPO3 gene).

By CGC Genetics in Portugal.

TNPO3
Specificity
100 %
Genes
13 %
Limb-Girdle Muscular Dystrophy (LGMD) Sequencing Panel.

By PreventionGenetics PreventionGenetics in United States.

GAA, TRIM32, VCP, PNPLA2, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, ANO5, MYOT, TRAPPC11, DNAJB6 , (...)

View the complete list with 13 more genes
Specificity
4 %
Genes
13 %
Limb Girdle Muscular Dystrophy Type 1F via the TNPO3 Gene.

By PreventionGenetics PreventionGenetics in United States.

TNPO3
Specificity
100 %
Genes
13 %
Comprehensive Neuromuscular Sequencing Panel.

By PreventionGenetics PreventionGenetics in United States.

AGL, GAA, GNE, TRIM32, CRYAB, VCP, CAVIN1, DPM3, PNPLA2, DPM1, ALG2, SQSTM1, ISCU, CHAT, PFKM, PYGM, GBE1, DPAGT1, DMD, CHRNE , (...)

View the complete list with 104 more genes
Specificity
1 %
Genes
13 %
Limb girdle muscular dystrophy Comprehensive panel.

By Connective Tissue Gene Tests in United States.

GAA, TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, FHL1, EMD, TRAPPC11 , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
13 %
Limb girdle muscular dystrophy Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

GAA, TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, FHL1, EMD, TRAPPC11 , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
13 %
Limb girdle muscular dystrophy NGS panel.

By Connective Tissue Gene Tests in United States.

GAA, TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, FHL1, EMD, TRAPPC11 , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
13 %
Muscle Weakness (Myopathy, Muscular Dystrophy).

By MGZ Medical Genetics Center in Germany.

TTR, ACAD9, ACADM, ACADS, AGL, ACADVL, TWNK, GAA, TUBB3, AMACR, CPT2, GNE, TRIM32, POLG, SLC25A4, GARS, RRM2B, MFN2, CRYAB, HADHA , (...)

View the complete list with 159 more genes
Specificity
1 %
Genes
13 %
Muscle Weakness Manifesting in Adulthood / Limb-Girdle Muscular Dystrophy (AD and AR).

By MGZ Medical Genetics Center in Germany.

ACADM, AGL, ACADVL, GAA, CPT2, GNE, TRIM32, POLG, RRM2B, CRYAB, HADHA, VCP, PNPLA2, TK2, HADHB, PUS1, ABHD5, LPIN1, ISCU, PYGM , (...)

View the complete list with 70 more genes
Specificity
2 %
Genes
13 %
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
13 %
Limb-Girdle Muscular Dystrophies Panel.

By CeGaT GmbH in Germany.

GAA, GNE, TRIM32, DPM3, DMD, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT , (...)

View the complete list with 14 more genes
Specificity
3 %
Genes
13 %
Limb-Girdle Muscular Dystrophy type 1.

By Laboratory of Human Genetics GENOMED Health Care Center in Poland.

LMNA, CAV3, DES, MYOT, DNAJB6, TNPO3, HNRNPDL
Specificity
15 %
Genes
13 %
Limb girdle muscular dystrophy 1F.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

TNPO3
Specificity
100 %
Genes
13 %
TNPO3.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

TNPO3
Specificity
100 %
Genes
13 %
Invitae Comprehensive Neuromuscular Disorders Panel.

By Invitae in United States.

GAA, CPT2, GNE, TRIM32, CRYAB, VCP, DPM3, PNPLA2, DPM1, ALG2, SQSTM1, TAZ, CHAT, DPAGT1, DMD, SMN1, CHRNE, DOK7, FKTN, NEB , (...)

View the complete list with 84 more genes
Specificity
1 %
Genes
13 %
Invitae Comprehensive Muscular Dystrophy Panel.

By Invitae in United States.

GAA, TRIM32, DPM3, PNPLA2, DPM1, DMD, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, ANO5, MYOT , (...)

View the complete list with 26 more genes
Specificity
3 %
Genes
13 %
Invitae Cardiomyopathy and Skeletal Muscle Disease Panel.

By Invitae in United States.

TTR, AGL, GAA, EYA4, CPT2, GNE, TRIM32, DSP, CRYAB, RAF1, VCP, DPM3, PNPLA2, DPM1, SQSTM1, TAZ, SLC22A5, DOLK, DMD, GLA , (...)

View the complete list with 93 more genes
Specificity
1 %
Genes
13 %
Invitae Limb-Girdle Muscular Dystrophy Panel.

By Invitae in United States.

GAA, TRIM32, PNPLA2, DMD, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, ANO5, MYOT, TRAPPC11, DNAJB6 , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
13 %
TNPO3.

By Fulgent Genetics Fulgent Genetics in United States.

TNPO3
Specificity
100 %
Genes
13 %
LGMD and Congenital Muscular Dystrophy Panel.

By Blueprint Genetics in Finland.

TRIM32, CRYAB, PNPLA2, DMD, FKTN, SGCA, SGCB, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, MYH7, ANO5, MYOT, SELENON, MEGF10 , (...)

View the complete list with 22 more genes
Specificity
3 %
Genes
13 %
Comprehensive Muscular Dystrophy / Myopathy Panel.

By Blueprint Genetics in Finland.

GAA, TRIM32, POLG, CRYAB, PNPLA2, SEPT9, DMD, FKTN, NEB, SGCA, SGCB, SGCG, CAPN3, LMNA, PABPN1, FKRP, CAV3, DYSF, TTN, DES , (...)

View the complete list with 53 more genes
Specificity
2 %
Genes
13 %
MUSCULAR DYSTROPHY, LIMB-GIRDLE:NGS NGS PANEL.

By Laboratorio de Genetica Clinica SL in Spain.

TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, ANO5, MYOT, TRAPPC11, DNAJB6, DAG1, PLEC, POMT2 , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
13 %
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1F (AUTOSOMAL DOMINANT).

By Laboratorio de Genetica Clinica SL in Spain.

TNPO3
Specificity
100 %
Genes
13 %
IL12RB1 Sequencing.

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

IL12RB1
Specificity
100 %
Genes
13 %
IL12RB1 Deletion/duplication analysis.

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

IL12RB1
Specificity
100 %
Genes
13 %
Immunodeficiency 30 (sequence analysis of IL12RB1 gene).

By CGC Genetics in Portugal.

IL12RB1
Specificity
100 %
Genes
13 %
IL-12 Receptor B1 Deficiency via IL12RB1 Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

IL12RB1
Specificity
100 %
Genes
13 %
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
13 %
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
13 %
Defects of phagocytosis Panel.

By CeGaT GmbH in Germany.

HFE, STAT1, SLC37A4, DTNBP1, HPS1, BLOC1S3, HPS6, HPS5, HPS4, HPS3, HAX1, AP3B1, TAZ, TCN2, SLC35C1, TCIRG1, CYBA, GATA2, SBDS, CYBB , (...)

View the complete list with 39 more genes
Specificity
2 %
Genes
13 %
Combined immunodeficiencies Panel.

By CeGaT GmbH in Germany.

TAP1, AK2, ADA, IL2RG, PNP, CHD7, RMRP, DCLRE1C, TBX1, SEMA3E, MAGT1, UNC119, DOCK8, JAK3, THBD, STIM1, CD40, CD40LG, CD3E, CD3D , (...)

View the complete list with 40 more genes
Specificity
2 %
Genes
13 %
Invitae Mendelian Susceptibility to Mycobacterial Disease Panel.

By Invitae in United States.

STAT1, GATA2, CYBB, SAMHD1, ADAR, MYD88, IFNGR1, IFNGR2, IRAK4, IL12RB1, TYK2, IL12B, ISG15, ACP5, STAT2, IRF8
Specificity
7 %
Genes
13 %
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
1 %
Genes
13 %
IL12RB1.

By Fulgent Genetics Fulgent Genetics in United States.

IL12RB1
Specificity
100 %
Genes
13 %
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
1 %
Genes
13 %
Severe Combined Immunodeficiency Panel.

By Blueprint Genetics in Finland.

PMS2, STAT1, TAP1, AK2, STAT3, ADA, IL2RG, PNP, BLM, RMRP, ATM, DCLRE1C, RTEL1, WAS, TBX1, MAGT1, UNC119, PARN, DOCK8, SH2D1A , (...)

View the complete list with 59 more genes
Specificity
2 %
Genes
13 %
Immunodeficiency Type 30 , Sequencing IL12RB1 Gene.

By Reference Laboratory Genetics in Spain.

IL12RB1
Specificity
100 %
Genes
13 %
IRF5.

By Fulgent Genetics Fulgent Genetics in United States.

IRF5
Specificity
100 %
Genes
13 %
IL12A.

By Fulgent Genetics Fulgent Genetics in United States.

IL12A
Specificity
100 %
Genes
13 %

Alternate names

Biliary Cirrhosis, Primary, 1; Pbc1 Is also known as pbc;hanot syndrome; pbc; primary biliary cirrhosis.



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