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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.
Neurodevelopmental delay with impaired glycolysis and lysosomal expansion disease is a condition describes children (and sometimes adults) who learn and grow more slowly than expected because...
Atypical Norrie disease due to monosomy Xp11.3 is a rare condition that happens when a small piece of the short arm of the X chromosome (region...
Atrial septal defect (ASD) means there is a hole in the wall (the septum) that separates the two top chambers of the heart (the right and...
Oculomotor apraxia (OMA) means the brain has trouble starting fast eye movements called saccades, especially when trying to look to the side on purpose. People often...
Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia is a rare, inherited brain and nerve disorder that starts in childhood. The main problems are poor balance and...
Ataxia-telangiectasia-like disorder 2 (ATLD2) is a very rare, inherited (autosomal recessive) brain and body condition. It happens when both copies of a gene called PCNA (proliferating-cell...
MRE11 (MRE11A)–related ataxia-telangiectasia–like disorder 1 (ATLD1) is a rare, inherited brain and body condition caused by harmful changes in the MRE11A gene. This gene makes a...
Ataxia-telangiectasia-like disorder (ATLD) is a very rare, inherited brain and body condition. It happens when both copies of a person’s MRE11 gene have harmful changes (variants)....
Ataxia-telangiectasia-like disorder 1 (ATLD1) is a rare, inherited brain condition that slowly damages the cerebellum—the part of the brain that controls balance, coordination, and eye movements....
Ataxia-tapetoretinal degeneration syndrome—better known today as spinocerebellar ataxia type 7 (SCA7) is a rare, inherited neurodegenerative disease in which a progressive cerebellar ataxia (unsteady movement, slurred...
Ataxia-photosensitivity-short stature syndrome (APSS) is a very rare, likely genetic condition. The classic triad is: (1) problems with balance and coordination (ataxia), (2) abnormally strong skin...
Ataxia-Pancytopenia Syndrome (ATXPC) is a rare, inherited disorder caused most often by changes (variants) in a gene called SAMD9L. “Ataxia” means problems with balance and coordination...
