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You searched for “X” in All. RX Search found 56,125 result(s) and checks doctor-selected, exact-title, synonym, and related matches.
Cerebellar ataxia with bilateral vestibulopathy syndrome is a rare brain and inner-ear disorder where two main problems happen together: damage in the cerebellum (the part of...
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome (CANVAS) is a rare brain and nerve disease that slowly gets worse over many years. In this...
Mesoaxial polydactyly of the fingers means there is an extra finger in the middle part of the hand, usually next to the index, middle, or ring...
Mesoaxial polydactyly (also called central polydactyly) means that a person is born with an extra finger or toe in the middle part of the hand or...
Cayman cerebellar ataxia (also called cerebellar ataxia, Cayman type) is a rare genetic (inherited) brain condition that usually starts from birth or early infancy. The main...
Cayman type cerebellar ataxia (often shortened to “Cayman ataxia”) is a rare inherited brain development condition that starts from birth or very early infancy. It mainly...
Hyperphalangy-clinodactyly of the index finger with Pierre Robin syndrome is the long, technical name for a very rare birth condition also called Catel-Manzke syndrome. In this...
Malignant paroxysmal ventricular tachycardia (VT) is a very dangerous type of fast heart rhythm that starts in the lower chambers of the heart, called the ventricles....
Cataract-ataxia-hearing loss syndrome (often called cataract-ataxia-deafness syndrome) is an extremely rare genetic disorder. Only a very small number of patients (two sisters in one family) have...
Cataract-ataxia-deafness syndrome is an extremely rare genetic disorder in which a person has three main problems together: cataracts present from birth (clouding of the eye lenses),...
PITX3 early-onset non-syndromic cataract is a rare genetic eye condition where a baby or young child develops a cloudy lens (cataract) because of harmful changes (mutations)...
Early-onset non-syndromic cataract caused by mutation in PITX3 is a rare genetic eye disease where the clear lens of the eye becomes cloudy in infancy or...
