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This Concept Map, created with IHMC CmapTools, has information related to: Unit 14, Altered structure of chromosomes like translocations, Autosomal dominant like Familial polyposis coli Familial hypercholesterolaemia Achondroplasia Huntington disease Myotonic dystrophy Neurofibromatosis, Altered number of chromosomes includes Polyploidy, genetic problems contributes to Obesity, Diseases due to expansion of tandem repeats such as Huntington disease Fragile-X syndrome Myotonic dystrophy, Autosomes including Trisomy 18 Edward's syndrome, genetic problems contributes to Metabolic disorders, Chromosomal abnormalities including Altered structure of chromosomes, Diagnosis of genetic disorders via Molecular analyses, Altered structure of chromosomes like isochromosome, Autosomes including Trisomy 21 Down syndrome and otehrs, Sex chromosomes includes Hermaphroditism (50% 46, XX) (others 46XY or 45X/46XY mosaics), Sex chromosomes includes XYY, Single gene diseases like X-linked recessive, Genetic disorders include Diagnosis of genetic disorders, Genetic disorders include Chromosomal abnormalities, Autosomes including Trisomy 13 Patau syndrome, Genetic disorders include Diseases due to expansion of tandem repeats, Genetic disorders include Multifactorial diseases, Altered structure of chromosomes like deletions