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 Turner Syndrome
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”.
Diagram of the disease
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.
Description of tetralogy of fallot
This article related 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 Tetralogy of Fallot, the single most common form of congenital heart disease that causes cyanosis (bluish discoloration from lack of oxygen).
For Rare Disease Day 2023, RELX's Global Head of Corporate Responsibility, Márcia Balisciano, speaks to Shiv Gaglani, CEO & Co-Founder of Osmosis.
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 pernicious anemia, a disease in which the body produces auto-antibodies against a stomach protein called Intrinsic Factor, causing B12 deficiency that cannot be resolved efficiently through oral intake.
This article related 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 precocious puberty, a condition that causes children to start puberty early, affecting one in five thousand children.
This content supports the SDG Goal 3: Good health and well-being and Goal 6: Clean water and sanitation by emphasizing the presence of pathogens, particularly virus, in the waste and leachate materials of some landfills, and also on the waste management, awareness, precaution, needed to be considered to overcome the diseases caused by viral particles.
This article ties 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 the rare disease Langerhans Cell Histiocytosis (LCH), a proliferation of abnormal histiocytes, which are inflammatory immune cells that constantly patrol the body for invaders and can infiltrate multiple body parts including the bones, skin and nervous system.
Diagram Achalasia
This article ties 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 the rare disease Achalasia, which involves damage to the nerves in the esophagus causing the lower esophageal sphincter, a circular muscle at the end of the esophagus, to be unable to relax. The resulting symptoms include difficulty swallowing and chest pain.

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