Features

Anemia of Chronic Disease
Elsevier
This article relates to SDG 3. This resource, created together by Osmosis and the National Organization for Rare Diseases (NORD), aims to increase the knowledge and awareness about Anemia of Chronic Disease.
Epidermolysis bullosa
Elsevier
This article relates to SDG 3. This resource, created together by Osmosis and the National Organization for Rare Diseases (NORD), aims to increase the knowledge and awareness about Epidermolysis Bullosa that can cause life-threatening infections as well as some forms of cancer.
Diagram of ovarian cancer
Elsevier
This article relates to SDG 3. This resource, created together by Osmosis and the National Organization for Rare Diseases (NORD), aims to increase the knowledge and awareness about Ovarian Cancer, a difficult to detect cancer in which only 2 in 10 cases are diagnosed at an early stage.
Graphic of gorlin syndrome
Elsevier
This article relates to SDG 3. This resource, created together by Osmosis and the National Organization for Rare Diseases (NORD), aims to increase the knowledge and awareness about Gorlin Syndrome, a mutation in a tumor suppressor gene is the root cause of proliferation of cancer cells, leading to basal cell carcinomas, abnormal cysts in the jaw, bone deformities, and several other manifestations.
Diagram of leprosy
Elsevier
This article relates to SDG 3. This resource, created together by Osmosis and the National Organization for Rare Diseases (NORD), aims to increase the knowledge and awareness about Leprosy, an ancient chronic infection disease that can affect the skin, eyes, and nervous system.
Elsevier
This podcast, relating to SDG 3, Health and Wellbeing, is part of the Elsevier celebration of the World Health Organization’s World Health Day whose aim is to promote health, keep the world safe and serve the vulnerable – so everyone, everywhere can attain the highest level of health and well-being. April 7th 2023 marks the WHO’s 75th anniversary of World Health Day, with a focus of improving public health for all.
Diagram of Turner Syndrome
Elsevier
This article relates to SDG 3. This resource, created together by Osmosis and the National Organization for Rare Diseases (NORD), aims to increase the knowledge and awareness about Turner Syndrome, a condition characterized by a partial or complete loss of one of the two X chromosomes in females. The manifestations of this can be quite variable, resulting in infertility and/or distinctive physical features such as a short stature, webbed neck, or a “shield chest”.
Elsevier
This article relates to SDG 3. This resource, created together by Osmosis and the National Organization for Rare Diseases (NORD), aims to increase the knowledge and awareness about Pierre-Robin Sequence, a rare congenital condition characterized by physical anomalies that result in making the newborn's breathing difficult.
Diagram of the disease
Elsevier
This article relates to SDG 3. This resource, created together by Osmosis and the National Organization for Rare Diseases (NORD), aims to increase the knowledge and awareness about retroperitoneal fibrosis, an inflammatory condition in which fiber-like tissue accumulates behind the peritoneum and causes lower back pain.

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