Informaţii despre

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

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Boli A-Z 3-Methylglutaconic Aciduria Acanthamoeba Keratitis Acquired Immunodeficiency Syndrome Acute Diarrhea Acute Respiratory Distress Syndrome Acute Vascular Insufficiency of Intestine Adult Dermatomyositis Adult-Onset Still's Disease Adult Respiratory Distress Syndrome Aggressive Periodontitis Aging Alcoholic Hepatitis Alcohol-Related Neurodevelopmental Disorder Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amaurosis Fugax Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Aniridia 1 Ankylosis Anorexia Nervosa 1 Anoxia Antiphospholipid Syndrome Antithrombin Iii Deficiency Aphthous Stomatitis Appendicitis Argininemia Arteriovenous Malformation Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Asphyxia Neonatorum Aspiration Pneumonia Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Telangiectasia Athetosis Atrioventricular Block Attention Deficit-Hyperactivity Disorder Autism Autism Spectrum Disorder Autoinflammation, Lipodystrophy, and Dermatosis Syndrome Back Pain Bacterial Meningitis Bacterial Vaginosis Bagassosis Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Protein Disease 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 Fracture Bone Inflammation Disease Brachydactyly, Type E1 Brain Injury Bronchopulmonary Dysplasia Bruxism Budd-Chiari Syndrome Burning Mouth Syndrome Burns Bursitis Cardiac Arrest Carotid Stenosis Central Nervous System Vasculitis Central Precocious Puberty Central Retinal Vein Occlusion Cerebral Atherosclerosis Cerebral Palsy, Ataxic, Autosomal Recessive Cerebral Sinovenous Thrombosis Cerebral Visual Impairment Cerebritis Cerebrovascular Disease Cervicitis Chagas Disease Chikungunya Chlamydia Cholangitis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction Chorioamnionitis Chronic Fatigue Syndrome Cleft Palate, Isolated Colonic Pseudo-Obstruction Commensal Bacterial Infectious Disease Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complex Regional Pain Syndrome Cone-Rod Dystrophy 2 Congenital Cytomegalovirus Congenital Methemoglobinemia Conjunctivitis Constipation Contact Dermatitis Cryptogenic Cirrhosis Cutis Laxa, Autosomal Recessive, Type Iiia Cyanosis, Transient Neonatal Cytomegalovirus Infection Demyelinating Disease Dengue Hemorrhagic Fever Dengue Shock Syndrome Dental Caries Developmental Coordination Disorder Developmental Dysplasia of the Hip 1 Diarrhea Diastrophic Dysplasia Down Syndrome Duodenal Obstruction Duodenitis Dyskinetic Cerebral Palsy Dysphagia Dystonia Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency Eales Disease Early-Onset Generalized Limb-Onset Dystonia Eclampsia Encephalitis Encephalopathy Endocarditis Endometritis Epilepsy Esotropia Euthyroid Sick Syndrome Exotropia Extrinsic Cardiomyopathy Factor V Deficiency Factor Viii Deficiency Fanconi Anemia, Complementation Group E Foot Drop Frontal Sinusitis Gangliocytoma Gastric Dilatation Gastroenteritis Gastroesophageal Reflux Gastroschisis Gingival Overgrowth Gingivitis Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Graft-Versus-Host Disease Growth Hormone Deficiency Head Injury Hellp Syndrome Hematopoietic Stem Cell Transplantation Hemiplegia Hemoglobin E Disease Hemorrhagic Fever Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatitis B Hereditary Spastic Paraplegia Hereditary Spastic Paraplegia 51 Hip Luxation Hip Subluxation Holocarboxylase Synthetase Deficiency Homocysteinemia Hypersomnia Hypertonia Hypoascorbemia Hypopituitarism Hypotonia Hypoxia Idiopathic Neutropenia Immune System Disease Incontinentia Pigmenti Infantile Hypotonia Infective Endocarditis Inferior Vena Cava Interruption Inflammatory Bowel Disease Inherited Congenital Spastic Tetraplegia Inherited Metabolic Disorder Intellectual Disability - Athetosis - Microphthalmia Intestinal Disease Intracranial Hypertension Ischemia Ischemic Optic Neuropathy Joint Disorders Juvenile Glaucoma Juvenile Rheumatoid Arthritis Kawasaki Disease Keratoconjunctivitis Sicca Kernicterus Lacrimal Apparatus Disease Laryngitis Laryngomalacia Lennox-Gastaut Syndrome Leptospirosis Lesch-Nyhan Syndrome Leukomalacia Lissencephaly 1 Listeriosis Livedoid Vasculopathy Lyme Disease Macular Dystrophy, Retinal, 1, North Carolina Type Mannose-Binding Lectin Deficiency Maple Syrup Urine Disease Marburg Hemorrhagic Fever Meningitis Meningococcemia Mesenteric Vascular Occlusion Methemoglobinemia Methemoglobinemia, Beta-Globin Type Microcephaly Microphthalmia Miller-Dieker Lissencephaly Syndrome Mirage Syndrome Mixed Cerebral Palsy Miyoshi Muscular Dystrophy 1 Moebius Syndrome Molybdenum Cofactor Deficiency Monocytic Leukemia Multiple Sclerosis Muscular Dystrophy Myelomeningocele Myiasis Myoclonus Myositis Myositis Ossificans Myotonic Dystrophy Natural Killer Cell Leukemia Neonatal Hypoxic and Ischemic Brain Injury Neonatal Stroke Nervous System Disease Neu-Laxova Syndrome 1 Neurodegeneration with Brain Iron Accumulation 2a Neurogenic Bladder Neuroleptic Malignant Syndrome Neuronal Migration Disorders Neuronitis Neuropathy Nonalcoholic Steatohepatitis Nonarteritic Anterior Ischemic Optic Neuropathy Obstructive Jaundice Oligohydramnios Opitz Gbbb Syndrome, Type I Osteomyelitis Osteoporotic Fracture Osteosclerotic Myeloma Otitis Media Pancreatitis, Hereditary Paracetamol Poisoning Parametritis Paraplegia Patent Foramen Ovale Pelizaeus-Merzbacher Disease Pericarditis Perinatal Necrotizing Enterocolitis Periodontal Disease Periodontitis Peritonitis Periventricular Leukomalacia Pertussis Pineal Cyst Placenta Disease Placental Abruption Pneumoconiosis Pneumonia Poems Syndrome Polyglucosan Body Myopathy 1 with or Without Immunodeficiency Polyhydramnios Polyposis, Gastric Pontocerebellar Hypoplasia Porencephaly Portal Vein Thrombosis Post-Thrombotic Syndrome Precocious Puberty Pre-Eclampsia Pregnancy Loss, Recurrent 1 Prostatitis Prosthetic Joint Infection Protein C Deficiency Protein S Deficiency Prothrombin Deficiency, Congenital Pulmonary Edema Pulmonary Embolism Pulmonary Sequestration Pulpitis Pyelonephritis Quadriplegia Rasmussen Encephalitis Recurrent Corneal Erosion Refractive Error Respiratory System Disease Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Pigmentosa 55 Rheumatic Heart Disease Rheumatoid Arthritis Sagittal Sinus Thrombosis Schizencephaly Scoliosis Scorpion Envenomation Seizure Disorder Serotonin Syndrome Severe Hemophilia a Severe Intellectual Disability and Progressive Spastic Paraplegia Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sialadenitis Sickle Cell Anemia Sleep Apnea Sleep Disorder Slipped Capital Femoral Epiphysis Sneddon Syndrome Spastic Cerebral Palsy Spastic Diplegia Spastic Diplegia Cerebral Palsy Spastic Hemiplegia Spasticity Spastic Monoplegia Spastic Paraparesis Spastic Paraplegia 28, Autosomal Recessive Spastic Paraplegia 2, X-Linked Spastic Paraplegia 47, Autosomal Recessive Spastic Paraplegia 50, Autosomal Recessive Spastic Paraplegia 52, Autosomal Recessive Spastic Quadriplegia Spinal Cord Infarction Spinal Cord Injury Spondylolisthesis Spondylolysis Spondylosis Stachybotrys Chartarum Stiff-Person Syndrome Strabismus Stroke, Ischemic Sudden Sensorineural Hearing Loss Superior Mesenteric Artery Syndrome Suprabulbar Paresis, Congenital Sveinsson Chorioretinal Atrophy Swallowing Disorders Synovitis Systemic Onset Juvenile Idiopathic Arthritis Thrombasthenia Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thumb Deformity Tonsillitis Toxic Shock Syndrome Toxoplasmoză Traumatic Brain Injury Tremor Trypanosomiasis Twin-to-Twin Transfusion Syndrome Typhoid Fever Uterine Anomalies Varicose Veins Vein Disease Viral Encephalitis Vulvar Vestibulitis Syndrome Xanthogranulomatous Pyelonephritis