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 autosomal recessive hearing loss without other health problems.
is an autosomal-recessive, nonsyndromic hearing loss (sensorineural), often congenital.
is autosomal recessive hearing loss without other medical features, usually from birth.
is an inherited (autosomal recessive) hearing loss without other health issues.
is a rare inherited hearing loss without other features, present at birth.
is an inherited hearing loss without other features, caused by gene changes.
is autosomal recessive, causing bilateral inner-ear (sensorineural) hearing loss without other features.
is an autosomal recessive, nonsyndromic hearing loss without other features.
is an autosomal recessive hearing loss without other features, often congenital.
is inherited hearing loss without other features; autosomal recessive, often congenital.
is an autosomal recessive, non-syndromic cause of sensorineural hearing loss.
is an inherited hearing loss without other features, autosomal recessive.
is an inherited sensorineural hearing loss without other clinical features.
is an inherited condition causing isolated sensorineural hearing loss, often from birth.
causes inner-ear (sensorineural) hearing loss without other features; autosomal recessive.
is a genetic, autosomal recessive hearing loss (sensorineural) without other features.
is a genetic, autosomal recessive hearing loss without other health issues.
is an inherited (autosomal recessive) condition causing early-onset, progressive hearing loss.
is an autosomal recessive genetic hearing loss without other features.
is inherited from both parents (autosomal recessive) hearing loss without other symptoms.
is an inherited hearing loss affecting hearing only, autosomal recessive.
is an autosomal recessive, non-syndromic hearing loss without other issues.
is inherited hearing loss without other symptoms (nonsyndromic), autosomal recessive.
is a rare autosomal recessive hearing loss without other features.