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Charcot–Marie–Tooth disease; CHARGE syndrome; Charles Bonnet syndrome; Chiari–Frommel syndrome; Chiasmal syndrome; Chilaiditi syndrome; Child sexual abuse accommodation syndrome; CHILD syndrome; childhood myelodysplastic syndrome; Childhood tumor syndrome; Chinese Restaurant Syndrome; Chromosomal deletion syndrome; Chromosome 5q deletion ...
This list is incomplete; you can help by adding missing items. ( May 2016 ) Fetal abnormalities are conditions that affect a fetus or embryo , are able to be diagnosed prenatally, and may be fatal or cause disease after birth.
Egg drop syndrome '76 (EDS '76) is a viral disease that affects birds, notably chickens, ducks, geese and swans. It is characterised by a sudden drop in production of eggs as well as its eggshell quality in apparent healthy laying birds.
The term childhood disease refers to disease that is contracted or becomes symptomatic before the age of 18 or 21 years old. Many of these diseases can also be contracted by adults. Some childhood diseases include:
List of medical symptoms. Medical symptoms refer to the manifestations or indications of a disease or condition, perceived and complained about by the patient. [1] [2] Patients observe these symptoms and seek medical advice from healthcare professionals.
Signs of gastrointestinal disease (Haemorrhagic Enteritis) include diarrhea, anorexia, melena and hematochezia. Anaemia and dehydration may develop secondary to this haemorrhagic enteritis. Signs of reproductive disease (Egg Drop Syndrome) include low egg production/hatching and the laying of abnormal eggs (size, shape, colour, texture).
The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child.
Cat eye syndrome; Caudal regression syndrome; Sotos syndrome Cerebral Gigantism; CHARGE syndrome; Chromosome 16 abnormalities; Chromosome 18 abnormalities; Chromosome 20 abnormalities; Chromosome 22 abnormalities; Cleft lip/palate; Cleidocranial dysostosis; Club foot; Congenital adrenal hyperplasia (CAH) Congenital central hypoventilation syndrome