Informaţii despre

Nume Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
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Clasificare globală Malacards Boli rare
Clasificare anatomică Malacards Boli endocrine

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Boli A-Z Acute Adrenal Insufficiency Adrenal Adenoma Adrenal Carcinoma Adrenal Cortical Adenoma Adrenal Cortical Hypofunction Adrenal Gland Hyperfunction Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete Adrenal Rest Tumor Aging Amenorrhea Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Autism 6 Berardinelli-Seip Congenital Lipodystrophy Blood Group--Ahonen Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Bulimia Nervosa 2 Conn's Syndrome Cytochrome P450 Oxidoreductase Deficiency Eating Disorder Endocrine Pancreas Disease Fetal Macrosomia Glucose Intolerance Hyperandrogenism Hypoadrenocorticism, Familial Leptin, Serum Level of, Quantitative Trait Locus 1 Lipoid Congenital Adrenal Hyperplasia Non-Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Obesity-Hypoventilation Syndrome Pancreas Disease Pituitary-Dependent Cushing's Disease Polycystic Ovary Syndrome Sex Differentiation Disease Sick Building Syndrome Steroid Inherited Metabolic Disorder Testicular Leydig Cell Tumor Thoracic Outlet Syndrome