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| Chromosomal: |
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| Single Gene |
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| Multifactorial |
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| Chromosomes |
| · DNA packages |
| · Nomenclature |
| Chromosome Number |
| · Euploidy |
| · Polyploidy |
| · Aneuploidy |
| Nondisjunction |
| · Meiosis I |
| · Meiosis II |
| Chromosome Structure |
| · Translocations |
| · Deletions |
| · Duplications |
| · Inversions |
| · Angelman syndrome |
| · Breast cancer |
| · Cri du Chat |
| · Di George syndrome |
| · Down syndrome |
| · Klinefelter |
| · Chronic Mylogenic Leukemia (CML) |
| · Prader-Willi |
| · Trisomy 13 |
| · Trisomy 18 |
| · Turner syndrome |
| · William syndrome |
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| · Dominant traits |
| · Recessive traits |
| · Androgen Insensitivity syndrome (AIS) |
| · Cystic Fibrosis |
| · Fragile X |
| · Huntington disease |
| · Phenylketonuria deficiency (PKU) |
| · Sickle Cell Anemia |
| · Tay-Sachs |
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| · Alcoholism |
| · Alzheimer |
| · Atherosclerosis |
| · Breast cancer |
| · Diabetes |
| · Schizophrenia |
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