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