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Nume Spastic Paraparesis
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Boli A-Z Adrenoleukodystrophy Adrenomyeloneuropathy Adult T-Cell Leukemia Aging Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Aneurysm Aniridia 1 Anorexia Nervosa 1 Aortic Aneurysm Arachnoid Cysts Arachnoiditis Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Autonomic Dysfunction Axonal Neuropathy Back Pain B-Cell Expansion with Nfkb and T-Cell Anergy Beta-Thalassemia 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 Brucellosis Cataract Cataract 2, Multiple Types Cerebellar Degeneration-Related Autoantigen 3 Cerebral Palsy Cerebritis Chronic Pain Congenital Hepatic Fibrosis Creutzfeldt-Jakob Disease Cutaneous T Cell Lymphoma Dementia Dermatitis Dysautonomia Dystonia Eales Disease Early-Onset Familial Alzheimer Disease Encephalopathy Epilepsy Exostosis Fibrous Histiocytoma Folliculitis Gastroesophageal Reflux Headache Associated with Sexual Activity Hemiplegic Migraine Hemoglobinuria Hepatic Adenomas, Familial Hepatitis Hepatitis C Hepatitis C Virus Hereditary Ataxia Hereditary Spastic Paraplegia Histiocytic Sarcoma Histiocytoma Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis Human Immunodeficiency Virus Type 1 Human T-Cell Leukemia Virus Type 1 Human T-Cell Leukemia Virus Type 2 Hydrocephalus Hyperekplexia Hyperlysinemia, Type I Hyperparathyroidism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Infective Dermatitis Associated with Htlv-1 Ischemia Lateral Sclerosis Leukemia Leukodystrophy Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Lupus Erythematosus Lyme Disease Lymphoma Machado-Joseph Disease Masa Syndrome Microcephaly Mitochondrial Disorders Mood Disorder Multiple Sclerosis Multiple System Atrophy 1 Muscular Dystrophy Myelitis Myoclonus Myopathy Myositis Neonatal Lupus Erythematosus Neuroaxonal Dystrophy Neuroendocrine Tumor Neurogenic Bladder Neuronitis Neuropathy Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive Oculodentodigital Dysplasia Optic Nerve Hypoplasia, Bilateral Osteochondroma Ovalocytosis, Southeast Asian Pancreatic Neuroendocrine Tumor Pancreatitis Paraplegia Paroxysmal Nocturnal Hemoglobinuria Phenylketonuria Pigmented Villonodular Synovitis Polymyositis Polyneuropathy Postpartum Depression Premature Menopause Premature Ovarian Failure 7 Primary Hyperparathyroidism Prion Disease Protein S Deficiency Psoriasis Psoriasis 13 Quinquaud's Decalvans Folliculitis Restless Legs Syndrome Sarcoma Seizures, Benign Familial Neonatal, 1 Sensorineural Hearing Loss Spastic Diplegia Spasticity Spastic Paraparesis and Deafness Spastic Paraplegia 15, Autosomal Recessive Spastic Paraplegia 20, Autosomal Recessive Spastic Paraplegia 23 Spastic Paraplegia 35, Autosomal Recessive Spastic Paraplegia 3, Autosomal Dominant Spastic Paraplegia 49, Autosomal Recessive Spastic Paraplegia 4, Autosomal Dominant Spastic Paraplegia 50, Autosomal Recessive Spastic Paraplegia 52, Autosomal Recessive Spastic Paraplegia 7, Autosomal Recessive Spastic Paraplegia 9 Spinal Arachnoiditis Spondylosis Sporadic Hyperekplexia Strongyloidiasis Suprabulbar Paresis, Congenital Synovitis Syphilis Syringohydromyelia Syringomyelia Systemic Lupus Erythematosus T-Cell Leukemia Thalassemia Thyroiditis Transverse Myelitis Tremor Tropical Spastic Paraparesis Vasculitis Villonodular Synovitis Vitamin B12 Deficiency Wells-Jankovic Syndrome Xanthomatosis