Disease Index

Laryngo-tracheo-esophageal cleft (LC) type 4 is a serious congenital respiratory tract anomaly characterized by a cleft extending into the thoracic trachea and possibly down to the carina, with respiratory distress

human disease

congenital malformation of the larynx in which there is failure of recanalization of the laryngotracheal tube during gestation

viral disease

human disease

human disease

human disease

human disease

human disease

Late-onset junctional epidermolysis bullosa is a subtype of junctional epidermolysis bullosa (JEB, see this term) occurring in childhood or young adulthood

human disease

human disease

human disease

human disease

human disease

human disease

motor neuron disease characterized by painless but progressive weakness and stiffness of the muscles of the legs

Lathosterolosis is an extremely rare inborn error of sterol biosynthesis characterized by facial dysmorphism, congenital anomalies (including limb and kidney anomalies), failure to thrive, developmental delay and liver disease

rare autosomal recessive genetic disorder associated with retinitis pigmentosa, spastic paraplegia, and mental disabilities

developmental defect during embryogenesis

a rare lipoprotein metabolism disorder characterized clinically by corneal opacities, and sometimes renal failure and hemolytic anemia, and biochemically by severely reduced HDL cholesterol

poisoning by lead in the body, especially affects the brain

retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness

Human disease

human disease

human disease

human disease

osteochondrosis that results in death and fracture located in hip joint