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 hereditary autosomal-dominant, progressive sensorineural hearing loss without other symptoms.
is an inherited hearing loss without other features, autosomal dominant.
is autosomal-dominant progressive sensorineural hearing loss without other symptoms.
is an autosomal-dominant inherited hearing loss without other features, often progressive.
is an autosomal dominant, progressive sensorineural hearing loss without other features.
is an autosomal dominant, nonsyndromic, progressive inner-ear (sensorineural) hearing loss.
is an inherited sensorineural hearing loss without other health problems, often progressive.
causes inherited, typically progressive hearing loss without other health problems.
is an autosomal-dominant, genetic hearing loss without other health features, often progressive.
is inherited hearing loss without other symptoms, often progressive and variable.
is a genetic condition causing sensorineural hearing loss without other symptoms.
is an inherited hearing loss that doesn't involve other body systems.
is inherited hearing loss without other features (nonsyndromic), autosomal dominant.
is genetic hearing loss without other features, inherited autosomal dominant.
is an inherited hearing loss without other symptoms, often progressive.
is an autosomal dominant, nonsyndromic inner ear (sensorineural) hearing loss.
is a dominantly inherited, nonsyndromic hearing loss with variable severity.
is an autosomal dominant, nonsyndromic hearing loss, usually progressive and bilateral.
is an autosomal-dominant hearing loss without other features, often progressive.
causes autosomal dominant, progressive inner-ear (sensorineural) hearing loss without other symptoms.
is an inherited hearing loss that runs in families, without other symptoms.
is an inherited, autosomal dominant sensorineural hearing loss without syndromic features.
is a genetic condition causing progressive, non-syndromic sensorineural hearing loss.
is a dominantly inherited hearing loss without other health issues, often progressive.
