Also known as:
21 hydroxylase deficiency, 21-OHD, 21-hydroxylase deficiency, CYP21 deficiency, adrenal hyperplasia 3, adrenal hyperplasia, congenital, due to 21-HYDROXYLASE deficiency, adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency, classic 21-OHD CAH, classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, congenital adrenal hyperplasia 1, congenital adrenal hyperplasia due to 21-hydroxylase deficiency, hyperandrogenism, Nonclassic type, due to 21-Hydroxylase deficiency
Also known as:
classic 21-OHD CAH, salt wasting form
Also known as:
classic 21-OHD CAH, simple virilizing form
Also known as:
classic CLAH
Also known as:
PKDYS, PKDYS1, Parkinsonism-dystonia, infantile, 1, classic DTDS, dopamine transporter deficiency syndrome
Also known as:
GALT deficiency, Galt deficiency, classic galactosemia, classical galactosemia, homozygous duarte-type, galactose-1-phosphate uridyltransferase deficiency, galactose-1-phosphate uridylyltransferase deficiency, galactosemia, galactosemia type 1, galactosemia, Duarte variant, galactosemia, classic, transferase deficiency
Also known as:
Chl, Hodgkin disease, Hodgkin lymphoma, susceptibility to, classic Hodgkin disease, classical Hodgkin lymphoma, classical Hodgkin's lymphoma, lymphoma, Hodgkin, classic