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July is Hemochromatosis Awareness Month

July 7, 2022 Jennifer Dykeman Leave a Comment

Hemochromatosis Awareness - ThinkGenetic

by Jennifer Dykeman, MMSc Candidate Many people might not even know they have Hemochromatosis, a common genetic condition that can be diagnosed through a simple blood test. In honor of… CONTINUE

Filed Under: Advocacy, Education Tagged With: autosomal dominant, autosomal recessive, CDC, Centers for Disease Control and Prevention, gene, genetic change, genetic condition, hemochromatosis awareness month, Hemochromatosis.org, Hereditary hemochromatosis, HFE, HH, iron, phlebotomy, The National Society of Genetic Counselors, therapeutic blood removal

Napoleon Bonaparte and Hereditary Cancer

April 10, 2017 Morgan Simmons, MMSc, CGC Leave a Comment

He who fears being conquered is sure of defeat. – Napoleon Bonaparte Today we know that there are hereditary cancer syndromes that predispose families to develop various types of cancer…. CONTINUE

Filed Under: Education Tagged With: Angelina Jolie, BRCA1, cancer, CDH1, E-cadherin, gene, hereditary cancer, Hereditary Diffuse Gastric Cancer, Morgan Simmons, Napoleon Bonaparte, No Stomach for Cancer, Parry Guildford, research, Society for Investigating Nature

Site Update for Week of 12/01/2016

December 1, 2016 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to anyone searching for answers on genetic diseases and… CONTINUE

Filed Under: Updates Tagged With: Acromegaly, Acyl-coa dehydrogenase, ADAMTSL4, Agammaglobulinemia, Alagille syndrome, Alkaptonuria, Campomelic dysplasia, Cartilage-hair hypoplasia, Ceroid lipofuscinosis, CHARGE syndrome, chromosome pairs, congenital heart defect, developmental delay, DNA, enzyme, Fabry, Gal-1-PUT, galactose-1-phosphate uridyl transferase, Galactosemia, gene, genetic condition, glucose, Glutaric acidemia, glycogen storage disease, growth hormone, Huntington, hypogonadotropic hypogonadism, Kallman syndrome, Leopard syndrome, Mosaic trisomy 14, Noonan syndrome, Otosclerosis, Pitt-Hopkins syndrome, pituitary gland, protein, PTHS, Rare Disease, rare genetic disorder, Rett syndrome, Robinow syndrome, Sandhoff disease, Sickle cell anemia, Spinal muscular atrophy, Stickler syndrome, sugar, SYNGAP1, triple X syndrome, Trisomy 13, Trisomy x, webbed neck, XXX

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