Informaţii despre

Nume Adrenoleukodystrophy
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Diffuse sclerosis; Disorders of fatty-acid metabolism
Clasificare anatomică Malacards Boli ale sistemului reproducator; Boli de piele; Boli endocrine; Boli neuronale

Vezi şi

Boli A-Z Abcd Syndrome Acatalasemia Acute Adrenal Insufficiency Adrenomyeloneuropathy Aging Agnosia Albinism-Deafness Syndrome Alopecia Alopecia, Androgenetic, 1 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Anton's Syndrome Aortic Valve Disease 2 Arthrochalasia Ehlers-Danlos Syndrome Aspartylglucosaminuria Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Attention Deficit-Hyperactivity Disorder Auditory Agnosia Autoimmune Lymphoproliferative Syndrome, Type V Autonomic Dysfunction Balo Concentric Sclerosis Bipolar Disorder Bipolar I Disorder Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Branchiootic Syndrome 1 Central Nervous System Disease Cerebral Degeneration Cerebritis Childhood-Onset Cerebral X-Linked Adrenoleukodystrophy Cholestasis-Lymphedema Syndrome Chondrodysplasia Punctata Syndrome Chromosome Xq28 Deletion Syndrome Cleft Larynx, Posterior Colitis Cone-Rod Dystrophy 2 Congenital Bile Acid Synthesis Defect Corpus Callosum, Agenesis of, with Abnormal Genitalia Cortical Blindness D-Bifunctional Protein Deficiency Deafness, Dystonia, and Cerebral Hypomyelination Deafness Enamel Hypoplasia Nail Defects Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Dementia Demyelinating Disease Dystonia Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency Encephalitis Endotheliitis Exhibitionism Fucosidosis Gaucher Disease, Type Iii Hematopoietic Stem Cell Transplantation Hemophilia Hemophilia a Hereditary Spastic Paraplegia Hurler Syndrome Hydrocephalus Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoadrenocorticism, Familial Hypogonadism Krabbe Disease Learning Disability Leber Hereditary Optic Neuropathy Leukodystrophy Lipid Storage Disease Loeys-Dietz Syndrome Malignant Spiradenoma Mannosidosis Meckel Syndrome, Type 1 Metachromatic Leukodystrophy Mitochondrial Dna Depletion Syndrome 4a Mulibrey Nanism Multiple Sclerosis Multiple System Atrophy 1 Muscular Atrophy Neonatal Adrenoleukodystrophy Nervous System Disease Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Iv, of Riccardi Neuroleptic Malignant Syndrome Neuronitis Neuropathy Ocular Motor Apraxia Olivopontocerebellar Atrophy Opitz Gbbb Syndrome, Type Ii Paraplegia Pericardial Effusion Pericarditis Peroxisomal Acyl-Coa Oxidase Deficiency Peroxisomal Biogenesis Disorders Peroxisomal Disease Peroxisome Biogenesis Disorder 1a Peroxisome Biogenesis Disorder 1b Peroxisome Disorders Pneumonia Polyneuropathy Premature Ovarian Failure 7 Primary Cerebellar Degeneration Primary Progressive Multiple Sclerosis Pseudomyxoma Peritonei Refsum Disease, Classic Refsum Disease, Infantile Form Rhizomelic Chondrodysplasia Punctata Spasticity Spastic Paraparesis Spinal Muscular Atrophy Spinocerebellar Degeneration Sudanophilic Cerebral Sclerosis Systemic Scleroderma Thyroiditis Tuberous Sclerosis Tuberous Sclerosis 1 Tumefactive Multiple Sclerosis Ulcerative Colitis Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Yemenite Deaf-Blind Hypopigmentation Syndrome Zellweger Spectrum Disorder Zellweger Syndrome