Inflammatory Bowel Disease 28, Autosomal Recessive; Ibd28

Clinical Features

Phenotypes and symptoms related to Inflammatory Bowel Disease 28, Autosomal Recessive; Ibd28

  • Fever
  • Inflammation of the large intestine
  • Colitis
  • Hematochezia
  • Enterocolitis
  • Folliculitis
  • Pyoderma
  • Perianal abscess

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Alternative names

Inflammatory Bowel Disease 28, Autosomal Recessive; Ibd28 Is also known as inflammatory bowel disease, early-onset, autosomal recessive.

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.


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Inflammatory Bowel Disease 28, Autosomal Recessive; Ibd28 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
IL10RA Deletion/duplication analysis.

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

IL10RA
Specificity
100 %
Genes
100 %
IL10RA Sequencing.

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

IL10RA
Specificity
100 %
Genes
100 %
IL10RA.

By Institute for Human Genetics University Clinic Freiburg (Germany).

IL10RA
Specificity
100 %
Genes
100 %
Early-onset inflammatory bowel disease, AR (sequence analysis of IL10RA).

By CGC Genetics (Portugal).

IL10RA
Specificity
100 %
Genes
100 %
IL-10 Receptor Gene.

By Immunology Diagnostics Laboratory Seattle Children's Research Institute (United States).

IL10RA, IL10RB
Specificity
50 %
Genes
100 %
IL10RA.

By Genome Diagnostics Laboratory University Medical Center Utrecht (Netherlands).

IL10RA
Specificity
100 %
Genes
100 %
Autoinflammatory panel.

By Genome Diagnostics Laboratory University Medical Center Utrecht (Netherlands).

SH3BP2, TNFRSF1A, LPIN2, IL36RN, NLRP3, NCSTN, NLRP12, NLRP7, PSENEN, NOD2, IL10, IL10RA, IL10RB, IL1RN, MEFV, MVK, PLCG2, PSMB8, PSTPIP1
Specificity
6 %
Genes
100 %
Autoinflammatory diseases Panel.

By CeGaT GmbH (Germany).

SH3BP2, TNFRSF1A, LPIN2, IL36RN, RBCK1, NLRP3, CARD14, NLRP12, SLC29A3, HFE, NOD2, IL10, IL10RA, IL10RB, IL1RN, MEFV, MVK, PLCG2, PSMB8, PSTPIP1
Specificity
5 %
Genes
100 %

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Sources and references

You can check the following sources for additional information.

OMIM MESH Rare Disease Symptoms Checker

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