BIOMAT Database Logo BIOMAT Database Logo

[Connection between congenital adrenal hyperplasia due to 21-hydroxylase deficiency and the HLA genotype]. 1983

M Dumić, and L Brkljacić, and C Krzisnik, and A Radica, and M Tajić, and A Kastelan

UI MeSH Term Description Entries
D008297 Male Males
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D005260 Female Females
D006680 HLA Antigens Antigens determined by leukocyte loci found on chromosome 6, the major histocompatibility loci in humans. They are polypeptides or glycoproteins found on most nucleated cells and platelets, determine tissue types for transplantation, and are associated with certain diseases. Human Leukocyte Antigen,Human Leukocyte Antigens,Leukocyte Antigens,HL-A Antigens,Antigen, Human Leukocyte,Antigens, HL-A,Antigens, HLA,Antigens, Human Leukocyte,Antigens, Leukocyte,HL A Antigens,Leukocyte Antigen, Human,Leukocyte Antigens, Human
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D006899 Mixed Function Oxygenases Widely distributed enzymes that carry out oxidation-reduction reactions in which one atom of the oxygen molecule is incorporated into the organic substrate; the other oxygen atom is reduced and combined with hydrogen ions to form water. They are also known as monooxygenases or hydroxylases. These reactions require two substrates as reductants for each of the two oxygen atoms. There are different classes of monooxygenases depending on the type of hydrogen-providing cosubstrate (COENZYMES) required in the mixed-function oxidation. Hydroxylase,Hydroxylases,Mixed Function Oxidase,Mixed Function Oxygenase,Monooxygenase,Monooxygenases,Mixed Function Oxidases,Function Oxidase, Mixed,Function Oxygenase, Mixed,Oxidase, Mixed Function,Oxidases, Mixed Function,Oxygenase, Mixed Function,Oxygenases, Mixed Function
D000312 Adrenal Hyperplasia, Congenital A group of inherited disorders of the ADRENAL GLANDS, caused by enzyme defects in the synthesis of cortisol (HYDROCORTISONE) and/or ALDOSTERONE leading to accumulation of precursors for ANDROGENS. Depending on the hormone imbalance, congenital adrenal hyperplasia can be classified as salt-wasting, hypertensive, virilizing, or feminizing. Defects in STEROID 21-HYDROXYLASE; STEROID 11-BETA-HYDROXYLASE; STEROID 17-ALPHA-HYDROXYLASE; 3-beta-hydroxysteroid dehydrogenase (3-HYDROXYSTEROID DEHYDROGENASES); TESTOSTERONE 5-ALPHA-REDUCTASE; or steroidogenic acute regulatory protein; among others, underlie these disorders. Congenital Adrenal Hyperplasia,Hyperplasia, Congenital Adrenal,Adrenal Hyperplasias, Congenital,Congenital Adrenal Hyperplasias,Hyperplasias, Congenital Adrenal
D013250 Steroid Hydroxylases Cytochrome P-450 monooxygenases (MIXED FUNCTION OXYGENASES) that are important in steroid biosynthesis and metabolism. Steroid Hydroxylase,Steroid Monooxygenases,Hydroxylase, Steroid,Hydroxylases, Steroid,Monooxygenases, Steroid
D013255 Steroid 21-Hydroxylase An adrenal microsomal cytochrome P450 enzyme that catalyzes the 21-hydroxylation of steroids in the presence of molecular oxygen and NADPH-FERRIHEMOPROTEIN REDUCTASE. This enzyme, encoded by CYP21 gene, converts progesterones to precursors of adrenal steroid hormones (CORTICOSTERONE; HYDROCORTISONE). Defects in CYP21 cause congenital adrenal hyperplasia (ADRENAL HYPERPLASIA, CONGENITAL). Cytochrome P-450 CYP21,Steroid 21-Monooxygenase,21-Hydroxylase,Cytochrome P-450 21-Hydroxylase,Cytochrome P-450 c21,Cytochrome P-450(c-21),Cytochrome P450c21,Progesterone 21-Hydroxylase,Steroid-21-Hydroxylase,21 Hydroxylase,Cytochrome P 450 21 Hydroxylase,Cytochrome P 450 CYP21,Cytochrome P 450 c21,P-450 c21, Cytochrome,Progesterone 21 Hydroxylase,Steroid 21 Hydroxylase,Steroid 21 Monooxygenase

Related Publications

M Dumić, and L Brkljacić, and C Krzisnik, and A Radica, and M Tajić, and A Kastelan
[Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: genotype-phenotype correlation].
January 2015, Acta medica portuguesa,
M Dumić, and L Brkljacić, and C Krzisnik, and A Radica, and M Tajić, and A Kastelan
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
June 2000, Endocrine reviews,
M Dumić, and L Brkljacić, and C Krzisnik, and A Radica, and M Tajić, and A Kastelan
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
January 2005, Journal for specialists in pediatric nursing : JSPN,
M Dumić, and L Brkljacić, and C Krzisnik, and A Radica, and M Tajić, and A Kastelan
Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.
September 2020, The New England journal of medicine,
M Dumić, and L Brkljacić, and C Krzisnik, and A Radica, and M Tajić, and A Kastelan
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
December 1990, The New England journal of medicine,
M Dumić, and L Brkljacić, and C Krzisnik, and A Radica, and M Tajić, and A Kastelan
[Congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
February 2004, Nihon rinsho. Japanese journal of clinical medicine,
M Dumić, and L Brkljacić, and C Krzisnik, and A Radica, and M Tajić, and A Kastelan
[Linkage analysis between HLA and GLOI with congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
February 1995, Pediatria polska,
M Dumić, and L Brkljacić, and C Krzisnik, and A Radica, and M Tajić, and A Kastelan
Genotype of Yupik Eskimos with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
March 1992, Human genetics,
M Dumić, and L Brkljacić, and C Krzisnik, and A Radica, and M Tajić, and A Kastelan
[Congenital adrenal hyperplasia due to 21-hydroxylase enzyme deficiency].
March 1996, Lijecnicki vjesnik,
M Dumić, and L Brkljacić, and C Krzisnik, and A Radica, and M Tajić, and A Kastelan
Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
October 1998, Clinical endocrinology,
Copied contents to your clipboard!