Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
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.
Inflammatory bowel disease
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Crohn disease-associated growth failure
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Inflammatory bowel disease 13
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Inflammatory bowel disease 25
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IL10RB
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Inflammatory bowel disease 28
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SEL1L
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| 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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