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Nume Fetal Macrosomia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli rare

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Boli A-Z Abdominal Obesity-Metabolic Syndrome 1 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 Abetalipoproteinemia Acanthosis Nigricans Acid-Labile Subunit Deficiency Acquired Metabolic Disease Acromegaly Adult Syndrome Aging Aland Island Eye Disease Al-Raqad Syndrome Alstrom Syndrome Amyloidosis Aa Aniridia 1 Anorexia Nervosa 1 Anovulation Apo a-I Deficiency Arcus Corneae Arteries, Anomalies of Atherosclerosis Susceptibility Autism 6 Beckwith-Wiedemann Syndrome Beckwith-Wiedemann Syndrome Due to Imprinting Defect of 11p15 Berardinelli-Seip Congenital Lipodystrophy Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System 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 Central Precocious Puberty Chylomicron Retention Disease Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Complete Androgen Insensitivity Syndrome Congenital Disorder of Glycosylation, Type It Congenital Generalized Lipodystrophy Coronary Heart Disease 1 Defective Apolipoprotein B-100 Diabetes Mellitus Diffuse Idiopathic Skeletal Hyperostosis Donohue Syndrome Dysbaric Osteonecrosis Endocrine Pancreas Disease Familial Hyperlipidemia Familial Lcat Deficiency Familial Partial Lipodystrophy Fasting Hypoglycemia Fatty Liver Disease Fish-Eye Disease Gallbladder Disease Gestational Diabetes Glucose Intolerance Glucose Metabolism Disease Growth Hormone Deficiency Hemihyperplasia, Isolated Hepatoblastoma Hyperalphalipoproteinemia 1 Hyperandrogenism Hypercholesterolemia, Familial Hyperglycemia Hyperinsulinemic Hypoglycemia Hyperinsulinemic Hypoglycemia, Familial, 2 Hyperinsulinism Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hyperpituitarism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertriglyceridemia, Familial Hypoalphalipoproteinemia, Primary Hypobetalipoproteinemia, Familial, 1 Hypoglycemia Hypoglycemic Coma Hypolipoproteinemia Hypopituitarism Hypoxia Insulin Autoimmune Syndrome Insulin-Like Growth Factor I Islet Cell Tumor Isolated Growth Hormone Deficiency, Type Ib Laron Syndrome Lecithin:cholesterol Acyltransferase Deficiency Leptin, Serum Level of, Quantitative Trait Locus 1 Leukodystrophy, Hypomyelinating, 3 Lipid Metabolism Disorder Lipodystrophy, Familial Partial, Type 2 Lipoprotein Glomerulopathy Lutheran Suppressor, X-Linked Mammographic Density Meninges Hemangiopericytoma Monocarboxylate Transporter 1 Deficiency Nutritional Deficiency Disease Obesity-Hypoventilation Syndrome Ocular Hyperemia Osteochondrosis Osteoporosis, Juvenile Pancreas Disease Pellagra Perlman Syndrome Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities Pituitary Adenoma 1, Multiple Types Polycystic Ovary Syndrome Polyhydramnios Prediabetes Syndrome Pseudopapilledema Rubeosis Iridis Salt and Pepper Developmental Regression Syndrome Secondary Adrenal Insufficiency Sheehan Syndrome Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Silver-Russell Syndrome Silver-Russell Syndrome Due to 11p15 Microduplication Silver-Russell Syndrome Due to an Imprinting Defect of 11p15 Sleep Apnea Slipped Capital Femoral Epiphysis Tangier Disease Type 1 Diabetes Mellitus 2 Umbilical Hernia Vaginitis Vitamin E, Familial Isolated Deficiency of