Informaţii despre

Nume Ehlers-Danlos Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli rare
Clasificari ICD10 Ehlers-Danlos syndrome
Clasificare anatomică Malacards Boli bucale; Boli de piele; Boli osoase
Boli din aceeaşi familie Autosomal Recessive Type Iv Ehlers-Danlos Syndrome; Ehlers-Danlos Syndrome Type 2; Ehlers-Danlos Syndrome, Type V; Type I Ehlers-Danlos Syndrome

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Boli A-Z Acroosteolysis Adenocarcinoma Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Androgen Insensitivity Syndrome, Mild Aneurysm Angioid Streaks Aniridia 1 Anorexia Nervosa 1 Aortic Aneurysm Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atlantoaxial Subluxation Atp6v0a2-Related Cutis Laxa Atrial Fibrillation Ayme-Gripp Syndrome Bladder Diverticulum Bladder Neck Obstruction Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brachial Plexus Neuropathy Brain Ischemia Brittle Bone Disorder Brittle Cornea Syndrome 2 Bronchiectasis Bruck Syndrome Bursitis Cardiac Tamponade Carotid Artery Occlusion Caspase 8 Deficiency Cerebrovascular Disease Cervical Incompetence Cervicitis Charcot-Marie-Tooth Disease Chondrosarcoma, Extraskeletal Myxoid Chromosome 6p Deletion Chromosome 6q Deletion Chronic Fatigue Syndrome Chronic Pain Cleft Lip Cleft Lip/palate with Abnormal Thumbs and Microcephaly Cleidocranial Dysplasia Clubfoot Collagen Disease Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Contractures Conjunctivochalasis Connective Tissue Disease Constipation Coronary Artery Dissection, Spontaneous Coronary Stenosis Cutis Laxa Cystic Adenomatoid Malformation of Lung Cystic Fibrosis Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome De Barsy Syndrome Dextrocardia Dilated Cardiomyopathy Down Syndrome Duodenal Atresia Duodenitis Dysautonomia Dyspepsia Ehlers-Danlos/osteogenesis Imperfecta Syndrome Ehlers-Danlos Syndrome, Arthrochalasia Type, 1 Ehlers-Danlos Syndrome, Classic-Like Ehlers-Danlos Syndrome, Classic Type, 1 Ehlers-Danlos Syndrome, Dermatosparaxis Type Ehlers-Danlos Syndrome, Hypermobility Type Ehlers-Danlos Syndrome, Kyphoscoliotic Form Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 1 Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 2 Ehlers-Danlos Syndrome, Periodontal Type, 1 Ehlers-Danlos Syndrome Progeroid Type Ehlers-Danlos Syndrome Type 2 Ehlers-Danlos Syndrome, Vascular Type Elastosis Perforans Serpiginosa Encephalocele Endocarditis Epilepsy Epithelial-Myoepithelial Carcinoma Epithelioid Hemangioendothelioma Factor Viii Deficiency Fanconi Anemia, Complementation Group E Fibromuscular Dysplasia Fibrous Dysplasia Flna-Related Periventricular Nodular Heterotopia Gastric Adenocarcinoma Geroderma Osteodysplastica Gingivitis Headache Helix Syndrome Hemangioendothelioma Hemarthrosis Hemochromatosis, Type 2a Hepatic Adenomas, Familial Hepatitis Hereditary Hemorrhagic Telangiectasia Hereditary Xanthinuria High Bone Mass Osteogenesis Imperfecta Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypermobile Ehlers-Danlos Syndrome Hypermobility Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypomelanosis of Ito Hypotonia Ichthyosis Vulgaris Intestinal Perforation Intestinal Pseudo-Obstruction Intracranial Aneurysm Intracranial Hypertension Intracranial Hypotension Ischemia Joint Laxity, Familial Juvenile Primary Osteoporosis Keloids Kyphoscoliotic Ehlers-Danlos Syndrome Larsen-Like Syndrome Laryngitis Leukodystrophy Loeys-Dietz Syndrome Lynch Syndrome Marden-Walker Syndrome Marfan Syndrome Meckel Diverticulum Mediastinitis Megacolon Melkersson-Rosenthal Syndrome Meningitis Monostotic Fibrous Dysplasia Morquio Syndrome Mowat-Wilson Syndrome Mucositis Multiple Chemical Sensitivity Multiple Sclerosis Muscular Atrophy Muscular Dystrophy Musculocontractural Ehlers-Danlos Syndrome Myocardial Infarction Myopathy Nail-Patella Syndrome Neurofibroma Neuropathy Obsessive-Compulsive Personality Disorder Occipital Horn Syndrome Olecranon Bursitis Orthostatic Intolerance Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteogenesis Imperfecta, Type Vii Osteogenesis Imperfecta, Type Viii Otosclerosis Palmoplantar Keratoderma, Epidermolytic Pancreas, Annular Pancreatitis Papillomatosis, Confluent and Reticulated Parkinsonism with Spasticity, X-Linked Periodontal Disease Periodontal Ehlers-Danlos Syndrome Periodontitis Peritonitis Periventricular Nodular Heterotopia Personality Disorder Pneumothorax Polyarteritis Nodosa Polymicrogyria Polyneuropathy Postural Orthostatic Tachycardia Syndrome Pseudoxanthoma Elasticum Radiculopathy Retinal Detachment Retinitis Rheumatic Disease Rheumatoid Arthritis Root Resorption Sciatic Neuropathy Scleral Staphyloma Scoliosis Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Single Ventricular Heart Situs Inversus Sleep Disorder Solitary Rectal Ulcer Syndrome Splenic Artery Aneurysm Spondylodysplastic Ehlers-Danlos Syndrome Spondyloepiphyseal Dysplasia Congenita Spondylolisthesis Spontaneous Intracranial Hypotension Subclavian Artery Aneurysm Superior Semicircular Canal Dehiscence Teeth, Supernumerary Tetraamelia Syndrome, Autosomal Recessive Thrombosis Tooth Disease Tracheobronchomegaly Tuberous Sclerosis Tuberous Sclerosis 1 Type I Ehlers-Danlos Syndrome Varicose Veins Vasculitis Vitamin E, Familial Isolated Deficiency of Von Willebrand Disease, Type 1 Wandering Spleen Xanthinuria