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