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Nume Chorea, Childhood-Onset, with Psychomotor Retardation
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Boli A-Z Aceruloplasminemia Acute Thyroiditis Aging Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Methylacetoacetic Aciduria Al-Raqad Syndrome Aneurysm Aniridia 1 Anorexia Nervosa 1 Anosognosia Antiphospholipid Syndrome Aphasia Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia-Oculomotor Apraxia 3 Athetosis Attention Deficit-Hyperactivity Disorder Autoimmune Hepatitis Autoimmune Polyendocrine Syndrome Basal Ganglia Calcification Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brainstem Auditory Evoked Responses Breast Cancer Cardiac Arrest Cataract Cavernous Malformation Central Retinal Artery Occlusion Cerebellar Atrophy, Developmental Delay, and Seizures Cerebellar Degeneration Cerebral Cavernous Malformations Cerebral Palsy Cerebritis Chorea, Benign Hereditary Chorea Gravidarum Chorea Minor Choreatic Disease Choreoacanthocytosis Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction Chronic Pain Churg-Strauss Syndrome Citrullinemia, Classic Complex Regional Pain Syndrome Congenital Hypothyroidism Conversion Disorder Cor Triatriatum Cor Triatriatum Sinister Creutzfeldt-Jakob Disease Cryopyrin-Associated Periodic Syndrome Curly Hair-Acral Keratoderma-Caries Syndrome Dementia Dentatorubral-Pallidoluysian Atrophy Diabetes and Deafness, Maternally Inherited Diabetes Mellitus Dilated Cardiomyopathy Dysautonomia Dystonia Encephalitis Encephalopathy Endocarditis Epilepsy Extrapontine Myelinolysis Focal Dystonia Fragile X Syndrome Frontotemporal Dementia Galactosemia Glioma Goiter Graves' Disease Hashimoto Thyroiditis Headache Hemolytic Anemia Hepatitis Herpes Simplex Herpes Simplex Encephalitis Holoprosencephaly Homocystinuria Huntington Disease Hydrocephalus Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius Hyperglycemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypoglycemia Hypoparathyroidism Iritis Ischemia Kluver-Bucy Syndrome Lateral Sclerosis Learning Disability Leber Hereditary Optic Neuropathy Leukemia Limbic Encephalitis Lingual-Facial-Buccal Dyskinesia Lung Cancer Lupus Erythematosus Manganese Poisoning Mcleod Syndrome Motor Neuron Disease Moyamoya Disease 1 Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Ii Mucopolysaccharidosis, Type Vii Multinodular Goiter Multiple System Atrophy 1 Muscular Atrophy Muscular Dystrophy Mycosis Fungoides Myelitis Myoclonus Myoclonus Epilepsy Myopathy Myxedema Neuronal Ceroid Lipofuscinosis Neuronitis Neuropathy Neurosyphilis Obsessive-Compulsive Disorder Olivopontocerebellar Atrophy Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to Oromandibular Dystonia Ovalocytosis, Southeast Asian Paine Syndrome Pandas Papilledema Papilloma Paroxysmal Choreoathetosis Pneumonia Polycythemia Polycythemia Vera Pontocerebellar Hypoplasia Progressive Multifocal Leukoencephalopathy Propionic Acidemia Pulmonary Hypertension Purpura Restless Legs Syndrome Retinal Artery Occlusion Retinitis Rheumatic Fever Rheumatic Fever-Related Antigen Rheumatic Heart Disease Schizophrenia Semilobar Holoprosencephaly Sjogren Syndrome Sleep Disorder Spasticity Spinocerebellar Atrophy Sydenham Chorea Systemic Lupus Erythematosus Temporal Lobe Epilepsy Tetraamelia Syndrome, Autosomal Recessive Thymoma Thyroiditis Tic Disorder Tick-Borne Encephalitis Transverse Myelitis Tremor Trichotillomania Uremia Vascular Disease Vasculitis Vitamin B12 Deficiency West Nile Virus Whipple Disease Xeroderma Pigmentosum, Complementation Group F