rs2032582 is a genetic variant on gene ABCB1 associated with Inflammatory bowel disease 13.
rs10876864 is a genetic variant on gene IKZF4 associated with Intelligence and Allergic disease.
rs11540652 is a genetic variant on gene TP53 associated with Li-fraumeni syndrome 1 and Multiple myeloma.
rs104894226 is a genetic variant on gene HRAS associated with Costello syndrome and Large congenital melanocytic nevus.
rs7274581 is a genetic variant associated with Alzheimer's disease.
rs10808546 is a genetic variant associated with Abdominal aortic aneurysm.
is a rare inherited condition causing developmental delay and intellectual disability.
is a rare inherited condition causing early developmental delay and intellectual disability.
is a genetic condition causing learning difficulties and delayed developmental milestones.
is a rare inherited condition causing developmental delays and intellectual disability.
is a rare inherited condition causing developmental delays and learning difficulties.
is a rare inherited condition causing intellectual disability and developmental delays.
is a rare autosomal recessive disorder causing developmental delays and intellectual disability.
is a rare inherited disorder causing developmental delay and intellectual disability.
is an autosomal recessive disorder causing lifelong learning and developmental difficulties.
is a rare autosomal recessive condition causing developmental delay and intellectual disability.
is a rare inherited condition causing lifelong learning and developmental challenges.
is a rare autosomal-recessive disorder causing developmental delays and intellectual disability.
is a rare inherited genetic condition causing developmental delay and intellectual disability.
is an autosomal recessive disorder causing developmental delay and intellectual disability.
is an autosomal recessive disorder causing developmental delays and intellectual disability.
is a rare autosomal recessive disorder causing intellectual disability and developmental delays.
is a rare disorder, inherited from both parents, causing intellectual disability.
is a rare autosomal recessive condition causing developmental delays and intellectual disability.
