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“Schistosoma-mansoni Infection”, Victor McKusick, Mendelian Inheritance in Man, 1966. 血管瘤-曼索尼感染。(SM1) icd10= B65. 1

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Here I present: “Schistosoma-mansoni Infection”, Victor McKusick, Mendelian Inheritance in Man’, 1966. 血管瘤-曼索尼感染。(SM1) icd10=B65.1

 

INTRODUCTION.

Schistosoma-mansoni is a water-borne parasite of humans and belongs to the group of blood flukes (Schistosoma). The adult lives in the blood vessels (mesenteric veins) near the human intestine. It causes intestinal schistosomiasis (similar to S. japonicum, S. mekongi, S. guineensis, and S. intercalatum). Clinical symptoms are caused by the eggs. As the leading cause of schistosomiasis in the world, it is the most prevalent parasite in humans. It is classified as a neglected tropical disease. As of 2021, the World Health Organization reports that 251.4 million people have schistosomiasis and most of it is due to Schistosoma-mansoni.

There is evidence that the susceptibility to Schistosoma-mansoni infection (SM1) is caused by mutation in the (SM1) gene on cytogenetic location 5q31-q33  and genomic coordinates 5:131,200,001-160,500,000.  The screenshot of the SM1 gene 29,300,000 bp (base pairs) of DNA sequence length is shown BELOW.  Nine (9) other genes besides SM1 in the 5q31-q33 cytogenetic location are listed BENEATH.

 


 

 

Coordinate  Symbol  Genomic Name
5:131,200,001  PDB4 Paget disease of bone 4
5:131,200,001  PFBI Plasmodium falciparum blood infection levels
5:131,200,001  PSORS11 Psoriasis susceptibility 11
5:131,200,001  RLS8 Restless legs syndrome, susceptibility to, 8
5:131,200,001  SM1 Schistosoma mansoni infection
5:131,210,052  CDC42SE2 CDC42 small effector 2
5:131,423,921  RAPGEF6 RAP guanine nucleotide exchange factor 6
5:131,641,714  FNIP1 Folliculin-interacting protein 1
5:131,806,990  MEIKIN Meiotic kinetochore factor
5:131,949,973  ACSL6 Acyl-CoA synthetase long-chain family member 6

 

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