Informaţii despre

Nume Paraplegia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Paraplegia, unspecified
Clasificare anatomică Malacards Boli neuronale

Vezi şi

Boli A-Z Ablepharon-Macrostomia Syndrome Achalasia-Addisonianism-Alacrima Syndrome Acute Transverse Myelitis Adenoma Adenosine Deaminase 2 Deficiency Adrenoleukodystrophy Adrenomyeloneuropathy Aging Alexander Disease Allan-Herndon-Dudley Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amyloidosis Amyloid Tumor Amyotrophic Dystonic Paraplegia Amyotrophic Lateral Sclerosis 2, Juvenile Amyotrophic Lateral Sclerosis Type 5 Anaplastic Oligoastrocytoma Anaplastic Oligodendroglioma Anauxetic Dysplasia 1 Aneurysm Angiolipoma Aniridia 1 Anorexia Nervosa 1 Anterior Spinal Artery Syndrome Anuria Aortic Aneurysm Aortitis Apparent Mineralocorticoid Excess Arachnoid Cysts Arachnoiditis Arteriovenous Fistula Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Asthma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Aural Atresia, Congenital Autonomic Dysfunction Autosomal Dominant Cerebellar Ataxia Autosomal Recessive Cerebellar Ataxia Axonal Neuropathy Back Pain B-Cell Lymphomas Beta-Thalassemia Biotinidase Deficiency 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 Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brachydactyly Breast Cancer Bronchogenic Cyst Burns Capillary Hemangioma Cardiac Arrest Carnosinemia Castleman Disease Cataract Cellular Schwannoma Cerebellar Degeneration Cerebral Atrophy Cerebral Palsy Cerebral Sinovenous Thrombosis Cerebritis Cerebrospinal Fluid Leak Cervicitis Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease, Axonal, Type 2t Chromophobe Adenoma Chromosome 18p Tetrasomy Chronic Meningitis Coarctation of Aorta Cobb Syndrome Cognitive Function 1, Social Collecting Duct Carcinoma Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cone-Rod Dystrophy 2 Congenital Contractures Conjunctivitis Conversion Disorder Cortical Blindness Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Cystinuria Darier-White Disease Dementia Demyelinating Polyneuropathy Dentatorubral-Pallidoluysian Atrophy Diastematomyelia Diffuse Idiopathic Skeletal Hyperostosis Distal Hereditary Motor Neuropathy, Type V Dysautonomia Dystonia Encephalitis Encephalopathy Ependymoma Epidermoid Cysts Epidural Abscess Epilepsy Epithelial Recurrent Erosion Dystrophy Erdheim-Chester Disease Essential Thrombocythemia Factor Vii Deficiency Factor Xii Deficiency Fanconi Anemia, Complementation Group E Fibrocartilaginous Embolism Fitzsimmons-Guilbert Syndrome Fitzsimmons Syndrome Foix-Alajouanine Syndrome Follicular Lymphoma Fragile X Syndrome Galactose Epimerase Deficiency Gas Gangrene Glioblastoma Glioblastoma Multiforme Glycogen Storage Disease Gout Gynecomastia Headache Associated with Sexual Activity Hemangioblastoma Hemangioma Hemangiopericytoma, Malignant Hematopoietic Stem Cell Transplantation Hemoglobin E-Beta-Thalassemia Syndrome Henoch-Schoenlein Purpura Hepatic Adenomas, Familial Hepatitis Hepatitis B Hepatocellular Carcinoma Hereditary Ataxia Hereditary Hemorrhagic Telangiectasia Hereditary Sensory Neuropathy Hereditary Spastic Paraplegia Histoplasmosis Homocarnosinosis Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Huntington Disease Hydrocephalus Hydronephrosis Hyperostosis Hyperparathyroidism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypertonia Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypokalemia Hypomelanotic Disorder Hypophosphatasia Hypophosphatemia Hypopituitarism Hypotonia Infant Gynecomastia Infantile-Onset Ascending Hereditary Spastic Paralysis Ischemia Juvenile Xanthogranuloma Klippel-Trenaunay-Weber Syndrome Lateral Sclerosis Leukemia Lipomatosis Locked-in Syndrome Lung Cancer Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphoma Machado-Joseph Disease Major Affective Disorder 8 Major Affective Disorder 9 Malignant Hypertension Malignant Teratoma Marfan Syndrome Masa Syndrome Mast Syndrome Mediastinitis Medulloblastoma Meningioma, Familial Meningitis Meningocele Meningococcal Meningitis Microcephaly Mitochondrial Complex V Deficiency, Nuclear Type 1 Mononeuropathy Morbid Obesity Motor Neuron Disease Multiple Sclerosis Muscular Atrophy Myelitis Myeloid Leukemia Myeloid Sarcoma Myeloma, Multiple Myoclonus Neurenteric Cyst Neuroaxonal Dystrophy Neuroblastoma Neurogenic Bladder Neurogenic Bowel Neuroma Neuromyelitis Optica Neuronitis Neuropathy Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive Neurosyphilis Norwegian Scabies Occipital Horn Syndrome Oculodentodigital Dysplasia Oligoastrocytoma Oligodendroglioma Orchitis Osteitis Fibrosa Osteomyelitis Overhydrated Hereditary Stomatocytosis Pancoast Tumor Pancytopenia Papillary Carcinoma Paraneoplastic Syndromes Paraplegia-Brachydactyly-Cone-Shaped Epiphysis Syndrome Pelizaeus-Merzbacher Disease Pelizaeus-Merzbacher-Like Disease Peroneal Neuropathy Phenylketonuria Pigmented Villonodular Synovitis Plasma Cell Leukemia Plasmacytoma Pleural Empyema Plexopathy Pneumococcal Meningitis Polyneuropathy Primary Cerebellar Degeneration Primary Hyperparathyroidism Primary Optic Atrophy Prostate Cancer Prostatitis Purine Nucleoside Phosphorylase Deficiency Purpura Quadriplegia Radiation Myelitis Ramer Ladda Syndrome Retinal Degeneration Retinitis Roussy-Levy Hereditary Areflexic Dystasia Sarcoma Scabies Schistosomiasis Seizures, Benign Familial Neonatal, 1 Seminoma Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sickle Cell Disease Sitosterolemia Sjogren-Larsson Syndrome Skeletal Tuberculosis Spastic Ataxia Spastic Ataxia, Charlevoix-Saguenay Type Spastic Diplegia Spasticity Spastic Paraparesis Spastic Paraplegia 10, Autosomal Dominant Spastic Paraplegia 11 Spastic Paraplegia 11, Autosomal Recessive Spastic Paraplegia 12, Autosomal Dominant Spastic Paraplegia 13, Autosomal Dominant Spastic Paraplegia 15, Autosomal Recessive Spastic Paraplegia 17 Spastic Paraplegia 17, Autosomal Dominant Spastic Paraplegia 18, Autosomal Recessive Spastic Paraplegia 20, Autosomal Recessive Spastic Paraplegia 24, Autosomal Recessive Spastic Paraplegia 26 Spastic Paraplegia 26, Autosomal Recessive Spastic Paraplegia 28, Autosomal Recessive Spastic Paraplegia 2, X-Linked Spastic Paraplegia 30, Autosomal Recessive Spastic Paraplegia 31, Autosomal Dominant Spastic Paraplegia 32, Autosomal Recessive Spastic Paraplegia 33, Autosomal Dominant Spastic Paraplegia 34, X-Linked Spastic Paraplegia 35, Autosomal Recessive Spastic Paraplegia 39, Autosomal Recessive Spastic Paraplegia 3a Spastic Paraplegia 3, Autosomal Dominant Spastic Paraplegia 4 Spastic Paraplegia 42, Autosomal Dominant Spastic Paraplegia 43, Autosomal Recessive Spastic Paraplegia 44, Autosomal Recessive Spastic Paraplegia 45, Autosomal Recessive Spastic Paraplegia 46, Autosomal Recessive Spastic Paraplegia 47, Autosomal Recessive Spastic Paraplegia 48, Autosomal Recessive Spastic Paraplegia 49, Autosomal Recessive Spastic Paraplegia 4, Autosomal Dominant Spastic Paraplegia 52, Autosomal Recessive Spastic Paraplegia 54, Autosomal Recessive Spastic Paraplegia 55, Autosomal Recessive Spastic Paraplegia 56, Autosomal Recessive Spastic Paraplegia 57, Autosomal Recessive Spastic Paraplegia 5a, Autosomal Recessive Spastic Paraplegia 61, Autosomal Recessive Spastic Paraplegia 6, Autosomal Dominant Spastic Paraplegia 78, Autosomal Recessive Spastic Paraplegia 7, Autosomal Recessive Spastic Paraplegia 8 Spastic Paraplegia 8, Autosomal Dominant Spastic Paraplegia 9a, Autosomal Dominant Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity Spastic Paraplegia, Optic Atrophy, and Neuropathy Spinal Cancer Spinal Cord Ependymoma Spinal Cord Infarction Spinal Cord Injury Spinal Meningioma Spinal Muscular Atrophy Spinal Stenosis Spinocerebellar Degeneration Splenic Marginal Zone Lymphoma Spondylitis Spondyloarthropathy Spondyloarthropathy 1 Spondylosis Superior Mesenteric Artery Syndrome Synovitis Syphilis Syphilitic Meningitis Syphilitic Myelopathy Syringomyelia Tabes Dorsalis Tarsal-Carpal Coalition Syndrome Telangiectasis Temporal Lobe Epilepsy Teratoma Tetrasomy 18p Thalassemia Thrombosis Thyroiditis Tooth Disease Transverse Myelitis Trichohepatoenteric Syndrome 1 Tropical Spastic Paraparesis Urethral Diverticulum Urethritis Vaginitis Vascular Disease Vasculitis Villonodular Synovitis Von Hippel-Lindau Syndrome Weber Syndrome Xanthomatosis X-Linked Complicated Spastic Paraplegia Type 1