Disease Index

Human disease

form of left renal vein compression

human disease

human disease

human disease

human disease

medical condition in which individuals have an excess of body fat

human disease

Congenital leptin deficiency is a form of monogenic obesity characterised by severe early-onset obesity and marked hyperphagia

human disease

human disease

Pro-opiomelanocortin (POMC) deficiency is a form of monogenic obesity resulting in severe early-onset obesity, adrenal insufficiency, red hair and pale skin

Prohormone convertase-I deficiency is the rarest form of monogenic obesity. The disorder is characterised by severe childhood obesity, hypoadrenalism, reactive hypoglycaemia, and elevated circulating levels of certain prohormones.

human disease

human disease

neurological injury in newborns

human disease

Occipital horn syndrome (OHS) is a mild form of Menkes disease (MD, see this term), a syndrome characterized by progressive neurodegeneration and connective tissue disorders due to a copper transport defect

human disease

macular degeneration that is characterized by a central cone dysfunction leading to a loss of vision with a normal fundus and normal fluorescein angiography findings

human disease

Human disease

human disease

gene involved in nephronophthisis, may be associated with ocular motor apraxia, Cogan type

ocular manifestation secondary to various neoplasms in which antibodies to antigens of the primary tumor cross-react with ocular antigens