Informaţii despre

Nume Aceruloplasminemia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Hallervorden-Spatz disease
Clasificare anatomică Malacards Boli ale ochiului; Boli de sânge; Boli neuronale

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Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Acute Disseminated Encephalomyelitis Acute Motor and Sensory Axonal Neuropathy Acute Motor Axonal Neuropathy Adenocarcinoma Adermatoglyphia Adie Pupil Adrenoleukodystrophy Aging Albinism Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alternating Hemiplegia of Childhood Aminoaciduria Anemia, Sideroblastic, and Spinocerebellar Ataxia Aneurysm Aniridia 1 Anorexia Nervosa 1 Anterior Horn Cell Disease Apraxia Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia Ataxia-Oculomotor Apraxia 3 Ataxia-Pancytopenia Syndrome Ataxia-Telangiectasia Atransferrinemia Autoimmune Disease Autoimmune Encephalitis Autoimmune Polyendocrine Syndrome Autonomic Dysfunction Autosomal Dominant Cerebellar Ataxia Autosomal Recessive Cerebellar Ataxia Autosomal Recessive Sideroblastic Anemia Axonal Neuropathy Babesiosis Bipolar Disorder Bleeding Disorder, Platelet-Type, 11 Blepharospasm, Benign Essential 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 Boucher-Neuhauser Syndrome Brain Injury Branchiootic Syndrome 1 Breast Cancer Camurati-Engelmann Disease Cataract Celiac Disease 1 Central Pontine Myelinolysis Cerebellar Ataxia and Neurosensory Deafness Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy, and Sensorineural Hearing Loss Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy and Sensorinural Hearing Loss Cerebellar Ataxia, Deafness, and Narcolepsy, Autosomal Dominant Cerebellar Ataxia, Early-Onset, with Retained Tendon Reflexes Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1 Cerebellar Ataxia, Mental Retardation and Dysequlibrium Syndrome Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome Cerebellar Degeneration Cerebellar Disease Cerebral Palsy, Ataxic, Autosomal Recessive Cerebritis Cerebrotendinous Xanthomatosis Cervical Dystonia Cervicitis Charcot-Marie-Tooth Disease, X-Linked Recessive, 3 Chickenpox Chikungunya Childhood Oligodendroglioma Cholangiocarcinoma Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chorioretinitis Choroiditis Chronic Active Epstein-Barr Virus Infection Ciliary Dyskinesia, Primary, 1 Cleft Palate, Isolated Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Ia Conjunctivitis Cortical Blindness Cranial Nerve Palsy Creutzfeldt-Jakob Disease Cystinuria Dementia Dentatorubral-Pallidoluysian Atrophy Desmoplastic Infantile Ganglioglioma Diabetes Insipidus Diabetes Mellitus Diffuse Alveolar Hemorrhage Dystonia Dystonia 11, Myoclonic Eales Disease Ectodermal Dysplasia Encephalitis Encephalomyopathy Encephalopathy Endotheliitis Epidermolysis Bullosa Epidermolysis Bullosa Dystrophica Epilepsy Epileptic Encephalopathy, Early Infantile, 36 Erdheim-Chester Disease Essential Tremor Extrapontine Myelinolysis Extraventricular Neurocytoma Familial Hemiplegic Migraine Fatal Familial Insomnia Focal Dystonia Friedreich Ataxia 1 Ganglioneuroma Gerstmann-Straussler Disease Gillespie Syndrome Gordon Holmes Syndrome Graves' Disease Hemangioblastoma Hemiplegia Hemiplegic Migraine Hemochromatosis, Type 1 Hemophagocytic Lymphohistiocytosis Hemosiderosis Hepatic Adenomas, Familial Hepatitis Hepatocellular Carcinoma Hereditary Ataxia Hereditary Spastic Paraplegia Herpes Zoster Herpes Zoster Ophthalmicus Histiocytosis Hydrocephalus Hyperferritinemia with or Without Cataract Hypochromic Microcytic Anemia Hypoglycemia Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypotonia Insulin-Like Growth Factor I Internuclear Ophthalmoplegia Intracranial Aneurysm Iron Metabolism Disease Ischemia Isoniazid Toxicity Juvenile-Onset Parkinson Disease Krabbe Disease Kufor-Rakeb Syndrome L-2-Hydroxyglutaric Aciduria Lambert-Eaton Myasthenic Syndrome Langerhans Cell Histiocytosis Laryngeal Abductor Paralysis Laryngitis Lateral Sclerosis Legionellosis Leptospirosis Leukemia Leukodystrophy Limbic Encephalitis Lung Combined Type Small Cell Carcinoma Lupus Erythematosus Lyme Disease Machado-Joseph Disease Majeed Syndrome Malaria Marden-Walker Syndrome Marinesco-Sjogren Syndrome Meningitis Meningitis and Encephalitis Meningococcal Meningitis Meningoencephalitis Metachromatic Leukodystrophy Metal Metabolism Disorder Mevalonic Aciduria Microcephaly, Epilepsy, and Diabetes Syndrome Miller Fisher Syndrome Mitochondrial Complex Iii Deficiency Motor Neuron Disease Movement Disease Mucopolysaccharidosis, Type Vii Multiple Sclerosis Multiple System Atrophy 1 Mumps Myoclonus Myoclonus Epilepsy Myofibrillar Myopathy Myopathy Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1 Narcolepsy Nephronophthisis Neural Crest Tumor Neuritis Neuroaxonal Dystrophy Neuroblastoma Neurodegeneration with Brain Iron Accumulation Neurodegeneration with Brain Iron Accumulation 1 Neurodegeneration with Brain Iron Accumulation 2a Neurodegeneration with Brain Iron Accumulation 2b Neurodegeneration with Brain Iron Accumulation 3 Neurodegeneration with Brain Iron Accumulation 4 Neurodegeneration with Brain Iron Accumulation 5 Neurodegeneration with Brain Iron Accumulation 6 Neuronal Intranuclear Inclusion Disease Neuronitis Neuropathy Neurosyphilis Obstructive Hydrocephalus Olivopontocerebellar Atrophy Opsoclonus-Myoclonus Syndrome Optic Neuritis Pancreatitis, Hereditary Pancytopenia Papilloma Papillomatosis, Confluent and Reticulated Paraneoplastic Cerebellar Degeneration Paraneoplastic Syndromes Paraplegia Parkinson Disease 15, Autosomal Recessive Early-Onset Parkinson Disease, Late-Onset Pellagra Pili Torti Plasmodium Falciparum Malaria Plasmodium Vivax Malaria Polydactyly Polyneuropathy Premature Ovarian Failure 1 Primary Cerebellar Degeneration Prion Disease Ptosis Refsum Disease, Classic Retinal Degeneration Retinitis Rosai-Dorfman Disease Sandhoff Disease Schizophrenia Seizures, Benign Familial Neonatal, 1 Sensorineural Hearing Loss Siderosis Sjogren Syndrome Sleep Disorder Small Cell Carcinoma Smith-Kingsmore Syndrome Spastic Ataxia Spastic Ataxia, Charlevoix-Saguenay Type Spastic Diplegia Spasticity Spastic Paraparesis Spastic Paraplegia 20, Autosomal Recessive Spastic Paraplegia 46, Autosomal Recessive Spastic Paraplegia 7, Autosomal Recessive Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinocerebellar Ataxia 1 Spinocerebellar Ataxia 12 Spinocerebellar Ataxia 13 Spinocerebellar Ataxia 15 Spinocerebellar Ataxia 17 Spinocerebellar Ataxia 18 Spinocerebellar Ataxia 19 Spinocerebellar Ataxia 2 Spinocerebellar Ataxia 28 Spinocerebellar Ataxia 31 Spinocerebellar Ataxia 36 Spinocerebellar Ataxia 4 Spinocerebellar Ataxia 6 Spinocerebellar Ataxia 7 Spinocerebellar Ataxia 8 Spinocerebellar Ataxia, Autosomal Recessive 1 Spinocerebellar Ataxia, Autosomal Recessive 8 Spinocerebellar Degeneration Sporadic Adult-Onset Ataxia of Unknown Etiology Squamous Cell Carcinoma Stiff-Person Syndrome Strabismus Striatonigral Degeneration Subcortical Arteriosclerotic Encephalopathy Superficial Siderosis Swayback Syne1-Related Autosomal Recessive Cerebellar Ataxia Systemic Lupus Erythematosus Teratoma Testicular Regression Syndrome Tetraamelia Syndrome, Autosomal Recessive Thalassemia Thrombocytopenia Thrombosis Thyroid Cancer Thyroiditis Toxocariasis Traumatic Brain Injury Tremor Typhoid Fever Undifferentiated Pleomorphic Sarcoma Virus Associated Hemophagocytic Syndrome Vitamin B12 Deficiency Vitamin E, Familial Isolated Deficiency of West Nile Virus Whipple Disease Wilson Disease Xanthomatosis Xeroderma Pigmentosum, Complementation Group F