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                    Genetic disorders, autosomal disorders, x-linked disorders/traits, etc.
                    
                 
                    
        
        
            
    
        
                            
        
                
        
            
                                
            
                
                                                | Genetic Disorders
                        
                                                                                    
                                                                                            | Caused by | Alleles inherited from parents |  
                                                                                            |  | Genetic mutations |  
                                                                                            |  | Chromosomal damage |  
                                                                                            |  | Environmental factors |  
                                                                                            |  | X-linked traits |  Types of Genetic Disorders
                        
                                                                                    
                                                                                            | Single-gene Disorders | One gene is affected by a mutation that is passed through parents; can be x-linked, autosomal, dominant or recessive |  
                                                                                            | Complex Disorders | More than one gene is affected by a mutation, not always passed through parents |  
                                                                                            | Chromosomal Disorders | Chromosomes (or parts of) are mutated or missing, not always passes through parents |  Chromosomal Disorders
                        
                                                                                    
                                                                                            | Down Syndrome (trisomy 21) |  
                                                                                            | Turner Syndrome (monosomy X) |  
                                                                                            | Edward Syndrome (trisomy 18) |  
                                                                                            | Patau Syndrome (trisomy 13) |  Complex Disorders
                        
                                                                                    
                                                                                            | Asthma |  
                                                                                            | Diabetes |  
                                                                                            | Hypertension |  
                                                                                            | Schizophrenia |  |  | Autosomal Disorders
                        
                                                                                    
                                                                                            | Autosome | A chromosome (not a sex chromosome) |  
                                                                                            | Autosomal Disorders | Diseases caused by genes on autosomes |  
                                                                                            | Autosomal Dominant | Disorders that are passed from one parent (homozygous dominant or heterozygous) |  
                                                                                            | Autosomal Recessive | Disorders that are passed from both parents (homozygous recessive) |  Autosomal Dominant Disorders
                        
                                                                                    
                                                                                            | Huntington's Disease | Neurological disorder; progressive degeneration of brain cells, muscle spasms, personality disorder |  
                                                                                            | Marfan Syndrome | Inherited disorder; affects the body's connective tissue causing disproportionately long limbs, weakened aorta, and poor eyesight |  
                                                                                            | BRCA 1 & BRCA 2 | Inherited in autosomal dominant pattern; hereditary breast cancer, |  Autosomal Recessive Disorders
                        
                                                                                    
                                                                                            | Cystic Fibrosis | Mucus in bronchial tubes and pancreatic ducts; shortened lifespan |  
                                                                                            | Sickle-cell Anemia | Mutated shape of red blood cells causing frequent blockages in blood vessels |  
                                                                                            | Tay-Sachs | Degeneration of central nervous system occurring in children |  X-Linked Traits
                        
                                                                                    
                                                                                            | Y Chromosome | Color blindness |  
                                                                                            |  | Hemophelia |  
                                                                                            | X Chromosome | Barr body |  | 
            
                            
            
            
        
        
        
        
        
            
    
        
          
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