Disease Index

human disease

human genetic disorder

medical condition

human disease

a rare autosomal recessive metabolic disorder

human disease

rare genetic disorder causing lack of fingerprints

adhesions or fibrosis of endometrium of uterus

neurological disorder characterized by a tonically dilated pupil

rare condition characterized by generalized obesity and fatty tumors in the adipose tissue.

human disease

medical emergency

human disease

adrenal cortex cancer that forms in the outer layer of tissue of the adrenal gland and that has material basis in abnormally proliferating cells derives from epithelial cells

hypopituitarrium that is characterized by a decreased or absent production of adrenocorticotropic hormone by the pituitary gland

human disease

Adrenomyeloneuropathy (AMN) is an adult form of the peroxisomal disease X-linked adrenoleukodystrophy (X-ALD, see this term), characterized by spastic paraparesia and often associated with peripheral adrenal insufficiency in males

rare genetic renal disease

hepatocellular carcinoma is characterized by hepatic mass, abdominal pain and, in advanced stages, jaundice, cachexia and liver failure and often develops in the setting of chronic necro-inflammation

hypophosphatasia that has material basis in a heterozygous mutation of ALPL on chromosome 1p36.12

human disease

leading to toxin-mediated infection with toxemia

human disease

Adult polyglucosan body disease (APBD) is a glycogen storage disease of adults characterized by progressive upper and lower motor neuron dysfunction, progressive neurogenic bladder and cognitive difficulties that can lead to dementia

Human disease

Human disease