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You searched for “Y” in All. RX Search found 56,145 result(s) and checks doctor-selected, exact-title, synonym, and related matches.
Congenital cystic eyeball, also called congenital cystic eye, is a very rare birth defect in which a cyst forms in the eye socket and the normal...
Congenital anophthalmos with cyst is a very rare birth defect of eye development. In this condition, a child is born without a normally formed eye in...
Congenital cystic eye is a very rare birth condition. In this condition, a cyst-like sac grows in the eye socket where the eye should normally form....
Distal arthrogryposis type 9 is an old name for congenital contractural arachnodactyly, often shortened to CCA. Many experts now prefer the name congenital contractural arachnodactyly because...
Beals-Hecht syndrome, also called congenital contractural arachnodactyly (CCA), is a rare inherited connective tissue disorder. It is usually caused by a change in the FBN2 gene,...
Congenital contractural arachnodactyly is a rare genetic connective tissue disorder that mainly affects the bones, joints, muscles, ears, and body shape. “Congenital” means it is present...
Congenital chylothorax means a baby is born with chyle collecting in the space around the lungs, called the pleural space. Chyle is a lymph fluid that...
Thyrotropin deficiency is also called TSH deficiency, central hypothyroidism, pituitary hypothyroidism, or secondary hypothyroidism. It happens when the pituitary gland does not make enough thyroid-stimulating hormone,...
Thyroid stimulating hormone deficiency means the pituitary gland does not make enough thyroid stimulating hormone, also called TSH. TSH is the signal that tells the thyroid...
Hypothalamic-pituitary hypothyroidism is usually called central hypothyroidism. It happens when the hypothalamus or the pituitary gland does not send the right hormone signals to the thyroid...
Congenital central hypothyroidism means a baby is born with low thyroid hormone because the brain does not send a strong enough signal to the thyroid gland....
Congenital cataracts-facial dysmorphism-neuropathy syndrome is a very rare inherited disorder. Doctors also call it CCFDN syndrome or CTDP1-related congenital cataracts, facial dysmorphism, and neuropathy. It mainly...
