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 non-syndromic hearing loss, usually progressive.
is an autosomal dominant inherited hearing loss without other health issues.
is an inherited condition causing progressive sensorineural hearing loss only.
causes inherited hearing loss without other features, varying from mild to severe.
is autosomal dominant, progressive sensorineural hearing loss without other symptoms.
is a hereditary, autosomal dominant sensorineural hearing loss without other features.
causes autosomal dominant, often progressive hearing loss without other features (nonsyndromic).
is an autosomal dominant, nonsyndromic hearing loss, usually progressive sensorineural.
is an inherited (autosomal dominant) hearing loss (sensorineural) without other features.
is an autosomal-dominant nonsyndromic hearing loss, usually progressive, sensorineural.
is a genetic, autosomal dominant hearing loss without other health problems.
causes autosomal dominant (one-parent inherited) hearing loss, often progressive, without other problems.
causes inherited, non-syndromic hearing loss, often progressive from high frequencies.
is an inherited autosomal-dominant hearing loss, often progressive, without other features.
is an autosomal dominant hearing loss without other symptoms, often progressive.
is inherited hearing loss without other features (nonsyndromic), autosomal dominant.
is an inherited, nonsyndromic sensorineural hearing loss, autosomal dominant, often progressive.
is an inherited condition causing progressive hearing loss without other features.
is autosomal dominant genetic sensorineural hearing loss, usually progressive, without other issues.
is an inherited, sensorineural hearing loss without other features, often progressive.
is an inherited, autosomal dominant hearing loss (sensorineural) without syndromic features.
is an inherited, nonsyndromic hearing loss that often worsens progressively.
is inherited in autosomal dominant pattern, causing progressive sensorineural hearing loss.
is an inherited, hearing-only (nonsyndromic) condition causing variably progressive hearing loss.