Hereditary angioedema is a rare genetic disorder characterized by severe episodic swelling due to accumulation of excessive body fluid (edema).

Duchenne muscular dystrophy is a rare and genetic disease characterized by progressive muscle weakness and degeneration/ loss (atrophy) of skeletal and cardiac muscles.

Fabry disease is a rare inherited lysosomal storage disorder that results from the accumulation of a specific type of fat in the body’s cells, called globotriaosyceramide (GL-3).

Myelodysplastic syndrome is a rare, heterogenous type of blood disorder that affects normal blood cell production in the bone marrow. Consequently,

Peripheral arterial disease characterizes a common circulatory problem caused by narrowed arteries that reduce blood flow to the limbs.

Congenital heart defects describe malformations of the heart that are existing at birth. Defects may involve the interior walls of the heart,

Pulmonary arterial hypertension (PAH) is a rare progressive disorder characterized by high blood pressure (hypertension) in the pulmonary arteries.

Pain defines a complex interaction between specialized nerves, the spinal cord and the brain. It is an important reaction of the nervous system which warns of possible injury.

Hematological disorders describe different kinds of pathological conditions that primarily affect the blood or blood-forming organs, e.g. red blood cells, white blood cells,

Peripheral T-cell lymphoma represents a rare aggressive (fast-growing) type of non-Hodgkin lymphoma, in which mature white blood cells, called T-cells,

Glioblastoma multiforme is the most common malignant and aggressive type of tumour that originates in the brain (primary brain tumour).

Chronic myeloid leukaemia is a type of cancer that affects the blood and bone marrow. In this condition the bone marrow produces too many granulocytes (white blood cells).