Congenital, Familial and Genetic Disorder Class

A class of disorders that encompasses conditions resulting from a congenital, familial hereditary trait or genetic abnormality as is manifested by a characteristic set of symptoms and signs. (NCI Thesaurus)

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Congenital Ventricular Tachycardia

An electrocardiographic finding of a tachycardia that originates in the ventricles that is present at birth.

Congenital Unilateral Cataract

Cataract in one eye that is present at birth.

Congenital Toxoplasmosis

Passed from mother to fetus.

Congenital Thyroid Gland Hypoplasia

Incomplete development of the thyroid gland in a newborn.

Congenital Thyroid Gland Disorder

A thyroid gland disorder present at birth. It includes thyroid gland aplasia and thyroid gland hypoplasia, both result in hypothyroidism.

Congenital Thyroid Gland Aplasia

Absence of the thyroid gland in a newborn.