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56,125 results found
You searched for “X” in All. RX Search found 56,125 result(s) and checks doctor-selected, exact-title, synonym, and related matches.
ALDH18A1-related autosomal recessive complex spastic paraplegia is a rare inherited nerve disease. It mainly affects the long nerve fibers that run from the brain to the...
Autosomal recessive complex spastic paraplegia type 9B (SPG9B) is a rare, inherited brain and nerve disease. It starts in childhood. The main sign is stiff, tight...
Autosomal recessive complex spastic paraplegia (SPG) due to Kennedy pathway dysfunction is a rare, inherited brain and spinal-cord disorder. “Spastic paraplegia” means stiff, tight, and weak...
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction is a genetic, childhood- or teen-onset nerve disease. “Autosomal recessive” means a child gets one faulty...
Autosomal recessive cerebellar ataxias (ARCAs) are a large family of rare, inherited brain disorders where both parents silently carry one faulty gene copy and a child...
Autosomal recessive cerebellar ataxia–saccadic intrusion syndrome is a rare, inherited movement disorder. “Autosomal recessive” means a person must receive one faulty gene from each parent to...
SCAR3 Spinocerebellar Ataxia Autosomal Recessive Type 3 is a rare inherited brain disorder that mainly affects the cerebellum (the balance and coordination center), and also damages...
Autosomal recessive spinocerebellar ataxia–blindness–hearing-loss syndrome is a rare genetic brain-nerve disorder. Children usually start life looking healthy, then develop problems with balance and coordination (ataxia). Over...
Autosomal recessive spinocerebellar ataxia type 3 (SCAR3/SCABD) is a rare, inherited brain and nerve disorder that starts in childhood. It mainly affects the cerebellum (the balance...
Autosomal recessive cerebellar ataxia–blindness–deafness syndrome (AR-CABDS) is a very rare inherited (genetic) brain and sensory disorder. Children usually start with balance and coordination problems because the...
Autosomal Recessive Cerebellar Ataxia due to GBA2 Deficiency is a rare inherited brain and nerve disorder in which both copies of a person’s GBA2 gene don’t...
Autosomal recessive cerebellar ataxia due to GBA2 deficiency is a rare, inherited brain disorder. It mainly affects the cerebellum, the part of the brain that controls...
