Disease Index

instance of renal tubular dysgenesis that is caused by a modification of the individual's genome

human disease

physical disorder characterized by pancreatic fibrosis, renal dysplasia and hepatic dysgenesis; it is usual fatal soon after birth

Renin-angiotensin-aldosterone system (RAAS)-blocker induced angioedema (RAE) is a type of acquired angioedema (AAE, see this term) characterized by acute edema in subcutaneous tissues, viscera and/or the upper airway

intellectual disability that is characterized by small head size (microcephaly), long narrow face, short stature, small testes, and intellectual deficit which follows X-linked inheritance and presents most often in males

medical condition

human disease

human disease

congenital structural abnormality of the respiratory system

organ system cancer located in the respiratory system that is characterized by uncontrolled cellular proliferation in the respiratory tract

form of cardiomyopathy in which the walls are rigid,and the heart is restricted from stretching and filling with blood properly

human disease

Human disease

human disease

human disease

Human disease

intermediate, locally aggressive and rarely metastasizing blood vessel neoplasm. It is characterized by the presence of hobnail endothelial cells and formation of arborizing vascular channels

human disease

human disease

human disease

retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss

Usher syndrome characterized by retinitis pigmentosa and onset of sensorineural hearing impairment in the teens that has material basis in mutation in the MTTS2 gene in the mitochondrial genome

human disease