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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.
Syndromic X-linked intellectual disability, Börjeson–Forssman–Lehmann type (BFLS) is a rare, inherited condition that mainly affects the brain, hormones, growth, and body shape. It is caused by...
Connective tissue disorder due to lysyl hydroxylase-3 deficiency (PLOD3-related disorder) is a rare genetic disease that affects the body’s collagen—the “scaffolding” protein that gives strength and...
Pseudoxanthoma Elasticum-Like Syndrome (PXE-Like Syndrome) is a rare inherited skin and connective-tissue condition that looks very similar to classic pseudoxanthoma elasticum (PXE). People develop loose, sagging,...
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency is a very rare inherited skin and blood-clotting disorder. The skin over the trunk and limbs...
Hypothyroidism–dysmorphism–postaxial polydactyly–intellectual disability syndrome is a rare genetic condition. Doctors most often call it Say-Barber-Biesecker-Young-Simpson syndrome (SBBYSS) or the Young–Simpson syndrome, a variant within the broader...
X-linked recessive Ohdo syndrome (Maat-Kievit-Brunner type, XLOS) is a very rare genetic condition that almost always affects boys. It is caused by changes (variants) in a...
Bleeding diathesis due to thromboxane synthesis deficiency is a rare bleeding problem. It happens when platelets do not make enough thromboxane A₂ (TXA₂), or cannot use...
Exstrophy of the urinary bladder sequence is a rare birth condition. It starts when a baby is growing in the womb. The lower belly wall does...
Congenital exstrophy of the urinary bladder is a birth defect. The lower belly wall does not close in the middle during early pregnancy. The front of...
Bladder exstrophy–epispadias–cloacal exstrophy complex (BEEC) is a group (a spectrum) of rare birth defects that affect the front wall of the belly and the lower urinary...
Bladder exstrophy is a rare birth defect. It happens when a baby’s lower tummy wall and the front wall of the bladder do not close before...
Ataxia–diabetes–goiter–gonadal insufficiency syndrome—better known as Bangstad syndrome—is an extremely rare, inherited disorder first described in 1989. It combines problems with movement and balance (ataxia), early insulin-resistant...
