Disease Index

benign or malignant neoplasm arising from the epithelial cells of an endocrine organ, e.g. pituitary gland adenoma, pituitary gland carcinoma, thyroid gland carcinoma, carcinoid tumor, or neuroendocrine carcinoma

type of disease affecting the endocrine system

human disease

germ cell cancer that has material basis in cells that line the yolk sac of the embryo

human disease

Human disease

disease linked to the female reproductive system

globe disease that is characterized by inflammation of the inside of the eye

inflammatory disease involving a pathogenic inflammatory response in the endothelium

an intermediate, rarely metastasizing blood vessel neoplasm characterized by the presence of lymphatic-like vascular channels and papillary endothelial proliferation

human disease

Eng-Strom syndrome is characterised by intrauterine growth retardation and intermittent locking of the finger joints. It has been described in two individuals: a mother and her daughter. The mode of transmission is autosomal dominant.

human disease

Goldmann-Favre syndrome (GFS) is a vitreoretinal dystrophy characterized by early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular edema, retinoschisis)

congenital disorder of digestive system

complication of coeliac disease

human disease

human disease

Human disease

human disease

Wells syndrome is characterised by the presence of recurrent cellulitis-like eruptions with eosinophilia

inflammation of the colon that is characterized by eosinic infiltration

esophagitis characterized by inflammation involving eosinophils located in esophagus

form of fasciitis, the inflammatory diseases that affect the fascia, the connective tissues surrounding muscles, blood vessels and nerves

Human disease

human disease

medical condition