https://padlet.com/zzbell1/11nu864ql865 Made with magic en-us 2018-11-08 14:48:28 UTC 2018-11-08 16:01:37 UTC hello@padlet.com zzbell1 https://padlet.com/zzbell1/11nu864ql865/wish/302089869 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. ]]> 2018-11-08 14:49:29 UTC https://padlet.com/zzbell1/11nu864ql865/wish/302089869 zzbell1 https://padlet.com/zzbell1/11nu864ql865/wish/302090315 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. ]]> 2018-11-08 14:50:02 UTC https://padlet.com/zzbell1/11nu864ql865/wish/302090315 zzbell1 https://padlet.com/zzbell1/11nu864ql865/wish/302091288 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.]]> 2018-11-08 14:50:41 UTC https://padlet.com/zzbell1/11nu864ql865/wish/302091288 zzbell1 https://padlet.com/zzbell1/11nu864ql865/wish/302091388 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.  ]]> 2018-11-08 14:50:49 UTC https://padlet.com/zzbell1/11nu864ql865/wish/302091388 zzbell1 https://padlet.com/zzbell1/11nu864ql865/wish/302091666 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.]]> 2018-11-08 14:51:10 UTC https://padlet.com/zzbell1/11nu864ql865/wish/302091666 zzbell1 https://padlet.com/zzbell1/11nu864ql865/wish/302093227 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.]]> 2018-11-08 14:53:08 UTC https://padlet.com/zzbell1/11nu864ql865/wish/302093227 zzbell1 https://padlet.com/zzbell1/11nu864ql865/wish/302103866 2018-11-08 15:07:08 UTC https://padlet.com/zzbell1/11nu864ql865/wish/302103866 zzbell1 https://padlet.com/zzbell1/11nu864ql865/wish/302109607 2018-11-08 15:14:03 UTC https://padlet.com/zzbell1/11nu864ql865/wish/302109607 zzbell1 https://padlet.com/zzbell1/11nu864ql865/wish/302114829 2018-11-08 15:20:43 UTC https://padlet.com/zzbell1/11nu864ql865/wish/302114829 zzbell1 https://padlet.com/zzbell1/11nu864ql865/wish/302131180 2018-11-08 15:41:22 UTC https://padlet.com/zzbell1/11nu864ql865/wish/302131180 zzbell1 https://padlet.com/zzbell1/11nu864ql865/wish/302135696 2018-11-08 15:48:20 UTC https://padlet.com/zzbell1/11nu864ql865/wish/302135696 zzbell1 https://padlet.com/zzbell1/11nu864ql865/wish/302139717 2018-11-08 15:54:10 UTC https://padlet.com/zzbell1/11nu864ql865/wish/302139717 zzbell1 https://padlet.com/zzbell1/11nu864ql865/wish/302141440 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. ]]> 2018-11-08 15:56:33 UTC https://padlet.com/zzbell1/11nu864ql865/wish/302141440 zzbell1 https://padlet.com/zzbell1/11nu864ql865/wish/302144575 2018-11-08 16:01:11 UTC https://padlet.com/zzbell1/11nu864ql865/wish/302144575