Also known as:
BFNS2, KCNQ3 benign neonatal seizures, benign neonatal seizures caused by mutation in KCNQ3, convulsions, benign familial neonatal, 2, seizures, benign familial neonatal, 2, seizures, benign familial neonatal, type 2, seizures, benign neonatal, 2
Also known as:
BFNS3, convulsions, benign familial neonatal, 3, seizures, benign familial neonatal, 3
Also known as:
Bfns, autosomal recessive, autosomal dominant form of benign neonatal seizures, convulsions benign familial neonatal dominant form, convulsions, benign familial neonatal, autosomal recessive, epilepsy, benign familial neonatal, autosomal recessive, seizures, benign familial neonatal, autosomal recessive
Also known as:
mtDNA depletion syndrome, encephalomyopathic form
Also known as:
Immunoglobin G subclass deficiency, selective IgG deficiency disease, selective IgG immunodeficiency, selective Immunoglobulin G subclass deficiency, selective deficiency of IgG, selective immunoglobulin G deficiency
Also known as:
SIgMD, selective IgM deficiency disease, selective immunoglobulin M deficiency
Also known as:
PRTH, hyperthyroidism, familial, due to inappropriate thyrotropin secretion, pituitary resistance to thyroid hormone, thyroid hormone resistance, selective pituitary
Also known as:
SHCB, SICI, self-improving collodion baby, self-improving congenital ichthyosis