Informaţii despre

Nume Marfan Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Marfan syndrome
Clasificare anatomică Malacards Boli ale ochiului; Boli cardiovasculare; Boli osoase

Vezi şi

Boli A-Z Achondroplasia Adie Pupil Afibrinogenemia Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Aminoaciduria Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Aneurysm Aniridia 1 Anorexia Nervosa 1 Aortic Aneurysm Aortic Aneurysm, Familial Abdominal, 1 Aortic Aneurysm, Familial Thoracic 1 Aortic Disease Aortic Valve Insufficiency Aortitis Arterial Tortuosity Syndrome Arteries, Anomalies of Arteriosclerosis Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 9 Atlantoaxial Subluxation Autosomal Dominant Polycystic Kidney Disease Bipolar Disorder Bleeding Disorder, Platelet-Type, 11 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 Breast Cyst Breast Reconstruction Brittle Bone Disorder Bronchiectasis Brucellosis Cardiac Tamponade Cataract Cerebritis Cerebrotendinous Xanthomatosis Cervicitis Charles Bonnet Syndrome Char Syndrome Chronic Actinic Dermatitis Chronic Pain Congenital Contractures Conjunctivitis Connective Tissue Disease Coronary Aneurysm Coronary Artery Aneurysm Dental Pulp Calcification Diaphragmatic Eventration Dilated Cardiomyopathy Down Syndrome Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome, Classic Type, 1 Endocarditis Endotheliitis Eosinophilic Granuloma Epidermolysis Bullosa Exotropia Factor Vii Deficiency Familial Abdominal Aortic Aneurysm Familial Thoracic Aortic Aneurysm and Dissection Fanconi Anemia, Complementation Group E Fibromatosis, Gingival, 1 Fibrous Dysplasia Focal Segmental Glomerulosclerosis Gastric Antral Vascular Ectasia Gigantism Headache Helix Syndrome Hemifacial Spasm Hemophilia Hemophilia a Hemopneumothorax Hepatic Adenomas, Familial Hepatitis Hereditary Hemorrhagic Telangiectasia Heritable Thoracic Aortic Disease Hernia, Hiatus Histidinemia Homocystinuria Hydronephrosis Hypermobility Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Heart Disease Hypertrophic Cardiomyopathy Hypertrophic Scars Hypoparathyroidism Hypophosphatemia Idiopathic Scoliosis Immune Suppression Immunodeficiency, Common Variable, 10 Infantile Scoliosis Infective Endocarditis Inguinal Hernia Interstitial Keratitis Intracranial Aneurysm Intracranial Hypotension Intrinsic Cardiomyopathy Ischemia Isolated Ectopia Lentis Keratoconus Late-Onset Focal Dermal Elastosis Lathyrism Left Ventricular Noncompaction Lens Subluxation Lipodystrophy Loeys-Dietz Syndrome Loeys-Dietz Syndrome 2 Long Qt Syndrome Marden-Walker Syndrome Marfanoid Hypermobility Syndrome Medullary Sponge Kidney Meningocele Mid-Dermal Elastolysis Migraine with Aura Multiple Self-Healing Squamous Epithelioma Multisystemic Smooth Muscle Dysfunction Syndrome Mungan Syndrome Mycosis Fungoides Myocardial Infarction Myocarditis Myopathy Myopathy, Proximal, and Ophthalmoplegia Neonatal Marfan Syndrome Neurofibromatosis, Type Iv, of Riccardi Ocular Cicatricial Pemphigoid Odontogenic Myxoma Open-Angle Glaucoma Orthostatic Intolerance Osteogenesis Imperfecta, Type Vii Ovarian Cyst Paranoid Schizophrenia Paraplegia Pectus Excavatum Periodontitis Phacogenic Glaucoma Pneumothorax Polycystic Kidney Disease Primary Optic Atrophy Protrusio Acetabuli Pseudoxanthoma Elasticum Pseudoxanthoma Elasticum-Like Papillary Dermal Elastolysis Pulmonary Emphysema Pulmonary Hypertension Pulmonary Subvalvular Stenosis Pulmonary Tuberculosis Pulmonic Stenosis Recessive Dystrophic Epidermolysis Bullosa Relapsing Polychondritis Renal Fibrosis Renovascular Hypertension Retinal Detachment Retinal Disease Retinitis Retinitis Pigmentosa Retroperitoneal Fibrosis Ring Chromosome 15 Ring Chromosome 2 Root Resorption Rutherfurd Syndrome Sarcoma Schizophrenia Scleroderma, Familial Progressive Scoliosis Senile Ectropion Severe Hemophilia a Skin Disease Sleep Apnea Sorsby Fundus Dystrophy Spinal Stenosis Spondylitis Spondyloarthropathy 1 Spontaneous Intracranial Hypotension Stiff Skin Syndrome Subclavian Artery Aneurysm Subvalvular Aortic Stenosis Superior Mesenteric Artery Syndrome Supravalvular Aortic Stenosis Tarlov Cysts Temple-Baraitser Syndrome Thrombophilia Thyroiditis Townes-Brocks Syndrome Tracheobronchomalacia Transient Hypogammaglobulinemia Transient Hypogammaglobulinemia of Infancy Tricuspid Valve Prolapse Trigeminal Neuralgia Turner Syndrome Urofacial Syndrome 1 Vascular Disease Vasculitis Ventricular Septal Defect Wandering Spleen Weill-Marchesani Syndrome Xanthomatosis