Disease Index

human disease

Human disease

Aminoacylase 1 deficiency (ACY1D) is an inborn error of metabolism marked by a characteristic pattern of urinary N-acetyl amino acid excretion and neurologic symptoms

human disease

Amish lethal microcephaly is a very rare syndrome characterized by extreme microcephaly and early death, within the first year

Human disease

amebiasis that involves infection of the intestine with Entamoeba histolytica trophozoites, which adhere to and kill colonic epithelial cells causing diarrhea with blood and mucus. The symptoms inlcude abdominal pain and fever

ampulla of Vater cancer that has material basis in abnormally proliferating cells derives from epithelial cells

human disease

metabolic disease involving abnormal deposited amyloid proteins

human disease

medical condition

rare neurodegenerative disease with amyotrophy and progressive paralysis

clinic-pathological entity that can be framed within frontotemporal dementia

human disease

neurodegenerative disease characterized by chronic, progressive amyotrophic lateral sclerosis and parkinsonism-dementia. Susceptibility to this disease is influenced by heterozygous mutation in TRPM7 on 15q21.2

anal canal cancer that derives from epithelial cells of glandular origin

anal canal cancer that derives from epithelial cells

anal canal cancer that derives from epithelial squamous cells

anus disease characterized by an abnormal connection between the epithelialised surface of the anal canal and the perianal skin

Congenital analbuminemia (CAA) is characterized by the absence or dramatic reduction of circulating human serum albumin (HSA)

astrocytoma that is characterized by cells with regular, round to oval nuclei

Human disease

Human disease

human disease

non-Hodgkin lymphoma involving aberrant T-cells

Human disease