Find disease guides, symptoms, medicines, lab tests, and patient-friendly medical resources.
56,145 results found
You searched for “Y” in All. RX Search found 56,145 result(s) and checks doctor-selected, exact-title, synonym, and related matches.
Congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome is an ultra-rare genetic disorder. In this condition, a baby is born with cataracts, which means the clear lens...
Myopathy, mitochondrial progressive, with congenital cataract and developmental delay is a very rare inherited mitochondrial disease. It is now often grouped under GFER-related primary mitochondrial disease....
Congenital Cataract-Progressive Muscular Hypotonia-Deafness-Developmental Delay Syndrome is an ultra-rare genetic mitochondrial myopathy. It is described by congenital cataract, progressive low muscle tone, sensorineural hearing loss, developmental...
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome is an ultra-rare genetic mitochondrial myopathy. In very simple words, it is a condition in which the body’s energy-making...
Basel-Vanagaite-Smirin-Yosef syndrome is a very rare inherited genetic disorder. It mainly affects brain development, learning, speech, growth, and several body systems. Most reported children have severe...
Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome is a very rare genetic disorder. It starts early in life. A baby may be born with cataracts in...
Congenital cataract-ichthyosis syndrome is an extremely rare inherited disorder in which a baby is born with cataract and ichthyosis together. A cataract means the clear lens...
Congenital respiratory-biliary fistula, also called congenital tracheobiliary fistula or congenital bronchobiliary fistula, is a very rare birth defect. In this condition, an abnormal tube connects part...
Congenital bronchobiliary fistula is a very rare birth defect. In this condition, an abnormal tube-like passage connects part of the breathing system, such as the trachea...
Inherited glutamine synthetase deficiency, also called congenital glutamine deficiency or GLUL-related glutamine synthetase deficiency, is an ultra-rare inherited metabolic disease caused by harmful changes in both...
Congenital brain dysgenesis due to glutamine synthetase deficiency is an ultra-rare inherited neurometabolic disease. It is also called GLND, congenital glutamine deficiency, inherited glutamine synthetase deficiency,...
Serpentine-like syndrome is a very rare congenital malformation syndrome. “Congenital” means the baby is born with it. It is mainly described by a very short esophagus...
