Ureteritis refers to a medical condition of the ureter that involves inflammation.One form is known as ureteritis cystica.Eosinophilic ureteritis has been observed.Ureteritis is often considered part of a urinary tract […]
List of articles in "Disease" category - Page 164
Fallopian tube cancer
Primary fallopian tube cancer (PFTC) often just tubal cancer is a malignant neoplasm that originates from the fallopian tube.
Lichenoid eruption
A lichenoid eruption is a skin disease characterized by damage and infiltration between the epidermis and dermis.Examples include lichen planus lichen sclerosus and lichen nitidus. It can also be associated […]
Björnstad syndrome
Björnstad syndrome is a congenital condition involving deafness and hair abnormalities.It was first characterized in 1965 in Oslo by prof. Roar Theodor Bjørnstad (1908–2002).It has been mapped to BCS1L.
MORM syndrome
MORM syndrome is an autosomal recessive congenital disorder characterized by mental retardation truncal obesity retinal dystrophy and micropenis.It is associated with INPP5E.
Nervous system disease
Nervous system disease refers to a general class of medical conditions affecting the nervous system.They can be divided into: Central nervous system disease in the CNS Peripheral neuropathy in the […]
Iridogoniodysgenesis dominant type
Iridogoniodysgenesis dominant type (type 1 IRID1) refers to a spectrum of diseases characterized by malformations of the irido-corneal angle of the anterior chamber of the eye. Iridogoniodysgenesis is the result […]
Gianotti–Crosti syndrome
Gianotti–Crosti syndrome (also known as Infantile papular acrodermatitis Papular acrodermatitis of childhood and Papulovesicular acrolocated syndrome) is a reaction of the skin to a viral infection. Hepatitis B and Epstein-Barr […]
Succinyl-CoA:3-oxoacid CoA transferase deficiency
Succinyl-CoA:3-oxoacid CoA transferase deficiency is an inborn error of ketone body utilization. Succinyl-CoA:3-oxoacid CoA transferase catalyzes the transfer of Coenzyme A from Succinyl-Coenzyme A to acetoacetate. It can be caused […]
Transaldolase deficiency
Transaldolase deficiency is a disease characterised by abnormally low levels of the Transaldolase enzyme. It is a metabolic enzyme involved in the pentose phosphate pathway. It is caused by mutation […]