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 sensorineural hearing loss without other symptoms, autosomal recessive.
is an autosomal recessive, non-syndromic hearing loss without other features.
is an autosomal recessive, nonsyndromic sensorineural hearing loss, often congenital.
causes autosomal recessive inner-ear (sensorineural) hearing loss without other features.
is a genetic condition causing nonsyndromic sensorineural hearing loss, autosomal recessive.
causes autosomal recessive, non-syndromic hearing loss, usually present from birth.
is a genetic, nonsyndromic inner-ear (sensorineural) hearing loss.
is a genetic, autosomal recessive hearing loss without other symptoms.
is an autosomal recessive condition causing isolated inner-ear (sensorineural) hearing loss.
is a genetic, autosomal recessive hearing loss without other features.
is an autosomal recessive disorder causing nonsyndromic, usually congenital hearing loss.
is autosomal recessive, nonsyndromic hearing loss, usually congenital or early-onset.
is a genetic hearing loss, usually without other medical problems.
is a congenital, inherited sensorineural hearing loss without other features.
is an inherited hearing loss (sensorineural) without other medical features.
is a rare inherited hearing loss without other medical features.
is an inherited, autosomal recessive hearing loss without other health features (nonsyndromic).
is a rare inherited, autosomal recessive hearing loss without other symptoms.
is inherited inner-ear (sensorineural) hearing loss without other medical features.
is an autosomal recessive, non-syndromic hearing loss, often from birth.
is an inherited, autosomal recessive, non-syndromic sensorineural hearing loss usually from birth.
is an inherited hearing loss without other medical features, autosomal recessive.
is an inherited, autosomal recessive, isolated hearing loss (nonsyndromic), usually sensorineural.
causes autosomal recessive sensorineural hearing loss without other systemic features.