Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
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Inflammatory bowel disease 28

Type 28 of genetic inflammatory bowel disease is an autosomal recessive disorder caused by mutations of the IL10RB gene which codes a component of the IL10 receptor.

Systematic

Inflammatory bowel disease
Crohn disease-associated growth failure
Inflammatory bowel disease 13
Inflammatory bowel disease 25
Inflammatory bowel disease 28
IL10RA
SEL1L

References:

1.

Glocker EO et. al. (2009) Inflammatory bowel disease and mutations affecting the interleukin-10 receptor.

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2.

Begue B et. al. (2011) Defective IL10 signaling defining a subgroup of patients with inflammatory bowel disease.

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3.

Mao H et. al. (2012) Exome sequencing identifies novel compound heterozygous mutations of IL-10 receptor 1 in neonatal-onset Crohn's disease.

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Update: Aug. 14, 2020
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