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Center for Nephrology and Metabolic Disorders
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Inflammatory bowel disease 25

Type 25 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
IL10RB
Inflammatory bowel disease 28
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.

None (2007) Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.

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4.

Silverberg MS et al. (2009) Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.

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5.

McGovern DP et al. (2010) Genome-wide association identifies multiple ulcerative colitis susceptibility loci.

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6.

Kugathasan S et. al. (2008) Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease.

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Update: Aug. 14, 2020
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