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 an inherited (autosomal dominant) condition causing intellectual and developmental disabilities.
is a rare genetic disorder causing developmental delays, intellectual disability, variable features.
is an autosomal dominant condition causing developmental delays and intellectual disability.
is a rare, autosomal dominant condition causing developmental delays and learning difficulties.
is an autosomal dominant neurodevelopmental disorder causing variable intellectual and developmental challenges.
is a rare autosomal dominant disorder causing developmental and learning difficulties.
is a genetic condition causing developmental delay, learning difficulties, and variable features.
is a genetic condition causing developmental delay, learning difficulties, autosomal dominant inheritance.
is a genetic condition causing developmental delays, learning difficulties, and variable features.
is a genetic condition causing developmental delays and intellectual disability; autosomal dominant.
is a genetic condition with autosomal dominant inheritance, affecting learning and development.
is an autosomal dominant genetic condition causing developmental delays and learning difficulties.
is a rare genetic condition causing intellectual disability and developmental delays.
is a rare genetic disorder causing intellectual disability and developmental delays.
is a genetic, autosomal-dominant condition causing developmental delay and intellectual disability.
is an autosomal dominant disorder causing developmental delay and intellectual disability.
is a rare inherited condition causing developmental delay and intellectual disability.
is a genetic condition causing developmental delay and intellectual disability, dominantly inherited.
is a genetic condition causing lifelong learning difficulties and developmental delays.
is a rare genetic condition causing developmental delays and learning difficulties.
is a genetic disorder causing developmental delay and intellectual disability.
