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Nume Body Mass Index Quantitative Trait Locus 12
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Clasificare globală Malacards Genetic diseases; Metabolic diseases

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Boli A-Z Aarskog-Scott Syndrome Ablepharon-Macrostomia Syndrome Acanthosis Nigricans Aceruloplasminemia Achalasia Achondroplasia Acinar Cell Carcinoma Acrocallosal Syndrome Acromegaly Actinomycosis Acute Cor Pulmonale Acute Graft Versus Host Disease Acute Insulin Response Acute Leukemia Acute Mountain Sickness Acute Myocardial Infarction Acute Pancreatitis Acute Promyelocytic Leukemia Acute Respiratory Distress Syndrome Adenocarcinoma Adenoma Adiponectin, Serum Level of, Quantitative Trait Locus 1 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency Adrenocortical Carcinoma, Hereditary Adult Lymphoma Adult Respiratory Distress Syndrome Aging Aicar Transformylase/imp Cyclohydrolase Deficiency Aland Island Eye Disease Alcohol Abuse Alcohol Dependence Alcoholic Pancreatitis Alexithymia Allergic Asthma Allergic Encephalomyelitis Allergic Hypersensitivity Disease Allergic Rhinitis Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alstrom Syndrome Alzheimer Disease 3 Amaurosis Fugax Amenorrhea Amyloidosis Anal Fistula Anauxetic Dysplasia 1 Androgen Insensitivity, Partial Anencephaly Aneurysm Angelman Syndrome Angel-Shaped Phalangoepiphyseal Dysplasia Angina Pectoris Angiosarcoma Aniridia 1 Anisomastia Anorexia Nervosa 1 Anovulation Antiphospholipid Syndrome Aortic Aneurysm Aortic Atherosclerosis Aortic Coarctation Aplastic Anemia Apnea, Obstructive Sleep Apolipoprotein C-Iii Deficiency Apparent Mineralocorticoid Excess Appendicitis Arteries, Anomalies of Arteriosclerosis Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Arthropathy Aspergillosis Aspiration Pneumonia Asthma Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrial Fibrillation Atrichia with Papular Lesions Attention Deficit-Hyperactivity Disorder Atypical Depressive Disorder Aural Atresia, Congenital Autism Autism Spectrum Disorder Autoimmune Hepatitis Autoimmune Neuropathy Autonomic Dysfunction Autonomic Neuropathy Ayazi Syndrome Ayme-Gripp Syndrome Azoospermia Back Pain Bardet-Biedl Syndrome Bardet-Biedl Syndrome 1 Bardet-Biedl Syndrome 10 Barrett Esophagus B-Cell Lymphomas Beckwith-Wiedemann Syndrome Beriberi Biemond Syndrome Biemond Syndrome Ii Biliary Tract Disease Bipolar Disorder Bipolar I Disorder Bladder Disease Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Group, Junior System Blount's Disease Body Mass Index Quantitative Trait Locus 1 Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 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 Bone Fracture Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Borderline Personality Disorder Borna Disease Bornholm Eye Disease Brachydactyly Brain Cancer Breast Cancer Breast Disease Breast Reconstruction Calcification of Joints and Arteries Calcinosis Calciphylaxis Camurati-Engelmann Disease Capillary Hemangioma Cardiac Arrest Carotid Intimal Medial Thickness 2 Carpal Tunnel Syndrome Cataract Cataract 5, Multiple Types Cauda Equina Syndrome Celiac Disease 1 Cellulitis Central Cord Syndrome Central Precocious Puberty Central Sleep Apnea Cerebral Artery Occlusion Cerebral Palsy Cerebritis Cerebrovascular Disease Ceroid Lipofuscinosis, Neuronal, 5 Cervical Cancer Cervical Intraepithelial Neoplasia Cervicitis Chagas Disease Charcot-Marie-Tooth Neuropathy Type 2a Chikungunya Childhood Leukemia Childhood Myocerebrohepatopathy Spectrum Cholangiocarcinoma Cholangitis Choledocholithiasis Cholelithiasis Cholestasis Chops Syndrome Chorioamnionitis Choroideremia Choroiditis Chromosome 1p36 Deletion Syndrome Chronic Fatigue Syndrome Chronic Laryngitis Chronic Pain Chronic Venous Insufficiency Ciliopathy Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Clear Cell Renal Cell Carcinoma Clopidogrel Resistance Cocaine Abuse Coffin-Lowry Syndrome Cohen-Gibson Syndrome Cohen Syndrome Colitis Colon Adenocarcinoma Colon Adenoma Colorectal Adenocarcinoma Colorectal Adenoma Colorectal Cancer Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Conduct Disorder Congenital Bile Acid Synthesis Defect Congenital Disorder of Glycosylation, Type Iic Congenital Hypothyroidism Congenital Leptin Deficiency Congenitally Corrected Transposition of the Great Arteries Congestive Heart Failure Conjunctivitis Constipation Coronary Artery Aneurysm Coronary Stenosis Corticosteroid-Binding Globulin Deficiency Cranial Nerve Malignant Neoplasm Craniopharyngioma Craniosynostosis with Fibular Aplasia Cystadenoma Cystic Fibrosis Cystic Kidney Disease Dacryoadenitis Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Degenerative Disc Disease Dementia Dental Caries Denys-Drash Syndrome Depersonalization Disorder Dermatitis Developmental Coordination Disorder Diabetes Insipidus Diabetes Mellitus Diabetes Mellitus, Insulin-Dependent Diabetes Mellitus, Noninsulin-Dependent Diabetic Autonomic Neuropathy Diabetic Cataract Diabetic Neuropathy Diabetic Polyneuropathy Diarrhea Diastolic Heart Failure Diastrophic Dysplasia Diffuse Idiopathic Skeletal Hyperostosis Diffuse Large B-Cell Lymphoma Dilated Cardiomyopathy Diverticulitis Dock2 Deficiency Donnai-Barrow Syndrome Double Discordia Down Syndrome Drug Dependence Ductal Carcinoma in Situ Dumping Syndrome Duodenal Ulcer Duodenitis Duodenogastric Reflux Dwarfism Dyspepsia Dysphagia Eating Disorder Eclampsia Ectopic Pregnancy Elephantiasis Empty Sella Syndrome Encephalocele Encephalopathy Endometrial Adenocarcinoma Endometrial Cancer Endotheliitis End Stage Renal Failure Entropion Epilepsy Epilepsy, Idiopathic Generalized Epithelial Recurrent Erosion Dystrophy Esophageal Atresia Esophageal Cancer Estrogen-Receptor Negative Breast Cancer Estrogen-Receptor Positive Breast Cancer Exocrine Pancreatic Insufficiency Exophthalmos Familial Colorectal Cancer Familial Lipoprotein Lipase Deficiency Familial Partial Lipodystrophy Fanconi Anemia, Complementation Group E Fasciitis Fatty Liver Disease Fecal Incontinence Fetal Macrosomia Fibrocalculous Pancreatopathy Focal Segmental Glomerulosclerosis Fragile X Syndrome Friedreich Ataxia 1 Fundus Albipunctatus Galactorrhea Gallbladder Cancer Gallbladder Disease Gas Gangrene Gastric Adenocarcinoma Gastric Cancer Gastric Cardia Adenocarcinoma Gastric Dilatation Gastritis Gastroduodenitis Gastroesophageal Reflux Gastroparesis Genitopatellar Syndrome Gestational Diabetes Gigantism Gingivitis Glioma Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Glomerulonephritis Glucagonoma Glucocorticoid Resistance, Generalized Glucose Intolerance Glucose Metabolism Disease Glycogen Storage Disease Goiter Gout Graft-Versus-Host Disease Granulomatous Hepatitis Growth Hormone Deficiency Gynecomastia Halothane Hepatitis Headache Helicobacter Pylori Infection Helix Syndrome Hemangioma Hemophilia Hemophilia a Hemorrhagic Proctocolitis Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hepatocellular Adenoma Hepatocellular Carcinoma Hereditary Wilms' Tumor Hernia, Hiatus Hidradenitis Hidradenitis Suppurativa Hinman Syndrome Histiocytosis Holoprosencephaly Homocysteinemia Horseshoe Kidney Human Immunodeficiency Virus Type 1 Hyaline Fibromatosis Syndrome Hydrocephalus Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius Hydronephrosis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperandrogenism Hypercholesterolemia, Autosomal Dominant, 3 Hyperglycemia Hyperinsulinemic Hypoglycemia Hyperinsulinemic Hypoglycemia, Familial, 2 Hyperinsulinism Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iv Hyperostosis Hyperparathyroidism Hyperproinsulinemia Hyperprolactinemia Hypersomnia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertension, Essential Hypertensive Heart Disease Hyperthyroidism Hypertrichosis Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertrophic Scars Hyperuricemia Hypoglycemia Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypolipoproteinemia Hypophosphatemic Bone Disease Hypopituitarism Hypospadias Hypothalamic Disease Hypotonia Hypoxia Ichthyosis Idiopathic Central Precocious Puberty Idiopathic Edema Ige Responsiveness, Atopic Ileitis Immune-Complex Glomerulonephritis Immunodeficiency 40 Immunodeficiency, Common Variable, 10 Immunodeficiency with Hyper-Igm, Type 3 Immunoglobulin E Concentration, Serum Infant Gynecomastia Infertility Inflammatory Bowel Disease Influenza Insulin-Like Growth Factor I Insulinoma Intermittent Claudication Interstitial Lung Disease Intracranial Hypertension Intrahepatic Cholestasis Intussusception Irritable Bowel Syndrome Ischemia Islet Cell Tumor Isolated Growth Hormone Deficiency Janus Kinase-3 Deficiency Jejunoileitis Keloids Keratoconjunctivitis Keratoconus Kidney Cancer Kwashiorkor Lactic Acidosis Langerhans Cell Histiocytosis Laron Syndrome Laryngeal Cleft Laryngitis Laugier-Hunziker Syndrome Learning Disability Lecithin:cholesterol Acyltransferase Deficiency Leopard Syndrome Leptin Receptor Deficiency Leukemia Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lichen Sclerosus Limb-Girdle Muscular Dystrophy Limb Ischemia Linitis Plastica Lipid Metabolism Disorder Lipid Storage Disease Lipodystrophy Lipodystrophy, Partial, Acquired Lipomatosis Lissencephaly 1 Liver Cirrhosis Liver Disease Logopenic Progressive Aphasia Long Qt Syndrome Lung Disease Lupus Erythematosus Lutheran Suppressor, X-Linked Lymphadenitis Lymphedema Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphocytic Choriomeningitis Lymphoma Lymphoma, Mucosa-Associated Lymphoid Type Lymphopenia Lymphosarcoma Lysosomal Acid Lipase Deficiency Malaria Male Infertility Malignant Hypertension Malignant Hyperthermia Marfan Syndrome Maturity-Onset Diabetes of the Young Mckusick-Kaufman Syndrome Mechanical Entropion Mediastinal Lipomatosis Mediastinitis Megaesophagus Megaloblastic Anemia Melanoma Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1 Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis Syndrome Meralgia Paresthetica Metabolic Acidosis Microcephaly Microcephaly, Epilepsy, and Diabetes Syndrome Microtia Microvascular Complications of Diabetes 1 Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia Migraine with Aura Migraine with or Without Aura 1 Mitochondrial Disorders Mitochondrial Import-Stimulating Factor Mohr-Tranebjaerg Syndrome Momo Syndrome Monocytic Leukemia Monogenic Diabetes Mononeuropathy of the Median Nerve, Mild Mood Disorder Morbid Obesity Mucinous Adenocarcinoma Mucolipidosis Ii Alpha/beta Multinodular Goiter Multiple Endocrine Neoplasia Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Personality Disorder Multiple Sclerosis Multiple Symmetrical Lipomatosis Mumps Mungan Syndrome Muscular Dystrophy Myasthenia Gravis Myelodysplastic Syndrome Myeloid Leukemia Myelomeningocele Myocardial Infarction Myopathy Myxedema Narcolepsy Necrobiosis Lipoidica Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Nephrosclerosis Nephrotic Syndrome Neural Crest Tumor Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neurogenic Hypertension Neurogenic Thoracic Outlet Syndrome Neuromuscular Disease Neuronitis Neuropathy Neutropenia Neutrophil Actin Dysfunction Neutrophilia, Hereditary Niemann-Pick Disease Night Blindness Nonalcoholic Steatohepatitis Obesity, Hyperphagia, and Developmental Delay Obesity-Hypoventilation Syndrome Obstructive Hydrocephalus Occipital Horn Syndrome Omenn Syndrome Open-Angle Glaucoma Opitz Gbbb Syndrome, Type I Optic Nerve Hypoplasia, Bilateral Orofacial Cleft Osgood-Schlatter's Disease Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteochondrosis Osteomalacia Osteopetrosis Osteoporotic Fracture Otitis Media Ouabain Resistance Ovarian Cancer Ovarian Cyst Ovarian Disease Overhydrated Hereditary Stomatocytosis Overnutrition Pachyonychia Congenita 1 Palmoplantar Carcinoma, Multiple Self-Healing Pancreas Disease Pancreatic Agenesis Pancreatic Cancer Pancreatitis Pancreatitis, Hereditary Pandas Papilledema Papillon-Lefevre Syndrome Papular Mucinosis Paraplegia Parathyroid Adenoma Patent Foramen Ovale Pathological Gambling Pediatric Hypertension Pediatric Multiple Sclerosis Pelvic Inflammatory Disease Penile Cancer Penis Agenesis Peptic Ulcer Disease Perinephritis Periodontal Disease Periodontitis Peripartum Cardiomyopathy Peritonitis Perlman Syndrome Personality Disorder Pertussis Phaeochromocytoma Pharyngitis Phenylketonuria Pheochromocytoma Pick Disease of Brain Pituitary Adenoma Pituitary Hormone Deficiency, Combined, 2 Pituitary Tumors Placental Abruption Placental Insufficiency Plantar Fasciitis Plasminogen Activator Inhibitor-1 Deficiency Plasmodium Falciparum Malaria Pneumonia Polycystic Ovary Syndrome Polycythemia Polydactyly Polydactyly, Postaxial, with Progressive Myopia Polyneuropathy Portal Hypertension Portal Vein Thrombosis Posterior Cerebral Artery Infarction Postpartum Depression Post-Thrombotic Syndrome Post-Traumatic Stress Disorder Potocki-Lupski Syndrome Pouchitis Prader-Willi Syndrome Precocious Puberty Prediabetes Syndrome Pre-Eclampsia Premature Ejaculation Primary Hyperparathyroidism Primary Lateral Sclerosis, Adult, 1 Primitive Portal Vein Thrombosis Proopiomelanocortin Deficiency Prostate Cancer Prostate Disease Prostatitis Prosthetic Joint Infection Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ic Pseudopseudohypoparathyroidism Psoriasis Psoriasis 13 Psoriatic Arthritis Pulmonary Disease, Chronic Obstructive Pulmonary Edema Pulmonary Embolism Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hypertension Purpura Pycnodysostosis Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome Rapp-Hodgkin Syndrome Recurrent Acute Pancreatitis Refsum Disease, Classic Renal Osteodystrophy Resting Heart Rate, Variation in Restless Legs Syndrome Restrictive Cardiomyopathy Retinal Degeneration Retinal Dystrophy and Obesity Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome Retinitis Retinitis Pigmentosa Retinoschisis 1, X-Linked, Juvenile Reye Syndrome Rheumatic Disease Rheumatoid Arthritis Rhinitis Rohhad Salt and Pepper Developmental Regression Syndrome Sarcoidosis 2 Schizoaffective Disorder Schizophrenia Schwartz-Jampel Syndrome, Type 1 Scleredema Sclerosing Cholangitis Senile Cataract Sensorineural Hearing Loss Severe Combined Immunodeficiency Short Bowel Syndrome Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sialadenitis Sickle Cell Anemia Siderosis Sinusitis Situs Inversus Sjogren-Larsson Syndrome Skeletal Dysplasias Skin Disease Sleep Apnea Sleep Disorder Slipped Capital Femoral Epiphysis Smith-Magenis Syndrome Social Phobia Spastic Cerebral Palsy Spasticity Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity Spinal Cord Injury Spinal Meningioma Spinal Stenosis Spondyloarthropathy Spondylolisthesis Spondyloocular Syndrome Squamous Cell Carcinoma Status Asthmaticus Steatorrhea Substance Abuse Succinic Semialdehyde Dehydrogenase Deficiency Sudden Sensorineural Hearing Loss Superior Mesenteric Artery Syndrome Sveinsson Chorioretinal Atrophy Syncope Syndromic X-Linked Intellectual Disability 7 Syringocystadenoma Papilliferum Systemic Lupus Erythematosus Systolic Heart Failure Taqi Polymorphism T Cell Deficiency Tendinopathy Tendinosis Teratoma Testicular Microlithiasis Tetralogy of Fallot Thoracic Outlet Syndrome Three M Syndrome 1 Thrombocytopenia Thrombophilia Thrombophlebitis Thrombosis Thyroid Cancer Thyroiditis Tongue Cancer Tonsillitis Tracheal Stenosis Transposition of the Great Arteries Transsexualism Transsexuality Tremor Trochlear Dysplasia Turner Syndrome Uniparental Disomy of Chromosome 2 Uremia Vaginitis Van Der Woude Syndrome 1 Varicocele Vascular Dementia Vascular Disease Vasculitis Venous Insufficiency Ventricular Fibrillation, Paroxysmal Familial, 1 Vertebrobasilar Insufficiency Viral Hepatitis Vitamin B12 Deficiency Voyeurism Werner Syndrome Wernicke Encephalopathy Williams-Beuren Syndrome Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome Wolffian Tumor Wolf-Hirschhorn Syndrome Woodhouse-Sakati Syndrome Yemenite Deaf-Blind Hypopigmentation Syndrome Zollinger-Ellison Syndrome