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“Inflammatory Bowel Syndrome”, Victor McKusick, Mendelian Inheritance in Man, 1966. (IBD3) icd10=K51.90

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Here I present: “Inflammatory Bowel Syndrome”, Victor McKusick, Mendelian Inheritance in Man’, 1966. (IBD3) icd10=K51.90

INTRODUCTION.

Inflammatory bowel disease (IBD) is a group of inflammatory conditions of the colon and small intestine, with Crohn’s disease and Ulcerative colitis being the principal types. 


Crohn’s disease
affects the small intestine and large intestine, as well as the mouth, esophagus, stomach and the anus, whereas Ulcerative colitis primarily affects the colon and the rectum.

There is evidence of genetic heterogeneity of inflammatory bowel disease (IBD3), including Crohn disease and ulcerative colitis is caused by mutation on cytogenetic location 6p21.3 and genomic coordinates 6:30,500,001-36,600,000. The screenshot of the IBD3 gene 6,100,000 bp (base pairs) of DNA sequence length is shown BELOW.  Nine (9) other genes besides IBD3 in the 6p21.3 cytogenetic location are listed BENEATH.

 



 

Coordinate  Symbol  Genomic Name
6:30,500,001  EJM3 Epilepsy, juvenile myoclonic 3
6:30,500,001  FL1 Follicular lymphoma, susceptibility to, 1
6:30,500,001  GPA Granulomatosis with polyangiitis
6:30,500,001  HLA-DRB3 Major histocompatibility complex, class II, DR beta-3
6:30,500,001  IBD3 Inflammatory bowel disease 3
6:30,500,001  IDDM1 Insulin-dependent diabetes mellitus-1
6:30,500,001  IGAD1 Immunoglobulin A deficiency
6:30,500,001  IGAT Immune response to synthetic polypeptide–IRGAT
6:30,500,001  IGLP1 Immune response to synthetic polypeptides-1
6:30,500,001  IGLP2 Immune response to synthetic polypeptides-2

 

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