Congenital Anomalies / Hereditary Conditions
Conditions
- albinism
- alpha-1 antitrypsin deficiency
- autosomal dominant polycystic kidney disease (previously known as: polycystic kidney disease)
- Charcot-Marie-Tooth disease
- Gaucher disease
- haemophilia
- hereditary haemochromatosis (previously known as: haemochromatosis)
- hereditary spherocytosis
- horseshoe kidney
- Huntington disease (previously known as: Huntington chorea)
- Marfan syndrome
- multiple osteochondromatosis
- osteogenesis imperfecta
- sickle-cell disorder
- von Willebrand disease
- Wilson disease