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Down Syndrome is not a inherited. The conditions of Down syndrome is caused by Trisomy 21. The chromosomal abnormality can occur as a random event during formation of reproduction cells from the parent. Down Syndrome wont have any conditions from an unaffected parent.

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Cystic Fibrosis runs in a families in an autosomes and its a recessive pattern.  both copies of the gene in each cell has mutations. A child can only get Cystic Fibrosis when the faulty CFTR  geng if from both of the parents is genetically passed down from others in their family that have Cystic Fibrosis.

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San Diego Chapter of the Cystic Fibrosis Foundation

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Animated video provide facts about cystic fibrosis. Created for San Diego Chapter of the Cystic Fibrosis Foundation's CureFinders in-school program.

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Tay sacs is inherited in an autosomal recessive manner. A person must have a mutation in both copies of the responsible gene in the cell. if both [parents are have Tay Sacs and they have a children together the child can probably get Tay Sacs.

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Tay-Sachs disease | Genetic and Rare Diseases

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There are two types of Hemophilia. we have Hemophilia A and Hemophilia B. They're both x-linked are recessive pattern. The genes are associated meaning the conditions are located on the X of the chromosomes. This genetic disorder can be passed from mother to son on the X of the chromosomes.

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PKU is inherited in families that's in an autosomal recessive pattern. If both parents have have a nonworking copy of a gene. If they have kids is a chance that the Baby might have PKU. Babies who have PUK are missing an Enzyme that's also known for Phenylalanine.

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Phénylcétonurie - Association Les Feux Follets

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PKU Kids video - Phenylketonuria explained to children

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People who have inherit two genes for sickle Hemoglobin meaning one individual cell from each parent. Possible chance that they have sickle cell. If the parents are thinking about having children and both parts have a gene of sickle cell the child can have a possible chance of having sickle cell.

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The heredity pattern for Huntington's Disease is one copy of the altered gene in each cell. Each cell is sufficient because of this disorder. people who have 27 to 45 CAG that's in the HTT gene don't develop Huntington but if they have children, the children may develop this type of disease.