Get Answer: Omim Online Mendelian Question Guide

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Original Question

OMIM, or Online Mendelian Inheritance in Man, is a comprehensive database of human genes and genomic phenotypes. # 1. Complete the chart below # 2. Select one condition listed below and provide a patient focused explanation on how the condition occurred describing type of mutation(s) at the molecular level. Incorporate lower health literacy levels in your explanation. See textbook (Page 35) and slides for examples of missense, nonsense, deletions & duplication explanations at a consumer level. DISORDER GENERAL DESCRIPTIONS MOLECULAR GENETICS: Include type(s) of mutations for each disorder Huntington Disease #143100 Cowden Syndrome I #158350 Von Willebrand Disease Type 1. #193400 . Cystic Fibrosis #219700 #602421 (Molecular genetics) . BECKER MUSCULAR DYSTROPHY #300376

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