Congenital afibrinogenemia
congenital afibrinogenemia n.
A hereditary disorder of blood coagulation in which little or no fibrinogen is present in the plasma.
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- Congenital alopecia
congenital alopecia n. A congenital condition in which all hair is absent.
- Congenital amputation
congenital amputation n. Loss of a fetal limb, usually the result of an intrinsic deficiency of embryonic tissue. Also called birth amputation, intrauterine amputation.
- Congenital anemia
congenital anemia n. See erythroblastosis fetalis.
- Congenital anomaly
congenital anomaly n. See birth defect.
- Congenital-defect
noun 1. . noun, Pathology. 1. any physical, mental, or biochemical abnormality present at birth. birth defect n. A physiological or structural abnormality that develops at or before birth and is present at the time of birth, especially as a result of faulty development, infection, heredity, or injury. Also called congenital anomaly.