Disease Index

human disease

human disease

toxic dose of colchicine

type of autoimmune hemolytic anemia

rare autoimmune disorder

autosomal dominant disease characterized by problems with regulating body temperature and other abnormalities affecting many parts of the body; it has material basis in mutations in the CRLF1 gene

human disease

osteogenesis imperfecta characterized by craniosynostosis, communicating hydrocephalus, ocular proptosis, marked postnatal growth failure, and distinctive facial appearance

eye disease characterized by missing pieces of tissue in structures that form the eye, such as the iris, retina, choroid or optic disc

human disease

congenital abnormality in which a part of the upper or lower eyelid tissue is missing

congenital or acquired defect characterized by the presence of a hole in or adjacent to the iris

human disease

medical condition

human disease

human disease

human disease

human disease

Colobomatous microphthalmia is a developmental disorder of the eye characterized by unilateral or bilateral microphthalmia associated with ocular coloboma

human disease

human disease

human disease

Human disease

Human disease

Colonic atresia is a congenital intestinal malformation resulting in a non-latent segment of the colon and characterized by lower intestinal obstruction manifesting with abdominal distention and failure to pass meconium in newborns

inability or decreased ability to see colour, or perceive colour differences, under normal lighting conditions

human disease