Search results for Genetic and rare disease guidance.

31 - 40 of 519 results for "Genetic and rare disease guidance."

• Hirschsprung's disease

  Hirschsprung's disease is a rare bowel condition that is mainly diagnosed in babies and young children.

• Chronic obstructive pulmonary disease (COPD)

  Find out about chronic obstructive pulmonary disease (COPD), including the symptoms, types, causes, how it's diagnosed and the treatment and support available.

• Alcohol-related liver disease (ARLD)

  NHS information about alcohol-related liver disease (ARLD), which is liver damage caused by drinking too much alcohol.

• Autosomal recessive polycystic kidney disease

  Autosomal recessive polycystic kidney disease (ARPKD) is a rare inherited childhood condition where the development of the kidneys and liver is abnormal.

• Bowen's disease

  Find out about the symptoms, causes and treatments for Bowen's disease, a very early and easily treatable form of skin cancer.

• Behçet's disease - Symptoms

  Read about the symptoms of Behçet's disease.

• Paget's disease of bone

  Find out about Paget's disease of bone, a condition where the normal cycle of bone renewal and repair is disrupted.

• Coronary heart disease - Treatment

  Read about the treatments for coronary heart disease (CHD).

• Prader-Willi syndrome

  Find out about Prader-Willi syndrome (PWS), which is a rare genetic condition that causes a wide range of physical symptoms, learning difficulties and behavioural challenges.

• Behçet's disease - Treatment

  Read about treating Behçet's disease.