Informaţii despre

Nume Pelizaeus-Merzbacher Disease
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Other sphingolipidosis
Clasificare anatomică Malacards Boli ale ochiului; Boli neuronale
Boli din aceeaşi familie Pelizaeus-Merzbacher-Like Disease

Vezi şi

Boli A-Z Adie Pupil Adrenoleukodystrophy Aging Allergic Encephalomyelitis Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Balo Concentric Sclerosis Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brainstem Auditory Evoked Responses Central Pontine Myelinolysis Cerebral Atrophy Cerebral Palsy Cerebritis Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease, Axonal, Type 2b Charcot-Marie-Tooth Disease, Demyelinating, Type 1a Charcot-Marie-Tooth Disease, Demyelinating, Type 1b Charcot-Marie-Tooth Disease, Demyelinating, Type 1d Charcot-Marie-Tooth Disease, Demyelinating, Type 1f Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 Charcot-Marie-Tooth Neuropathy Type 1 Chronic Inflammatory Demyelinating Polyradiculoneuropathy Cone-Rod Dystrophy 2 Congenital Hypomyelination Neuropathy Demyelinating Polyneuropathy Epithelial Recurrent Erosion Dystrophy Fanconi Anemia, Complementation Group E Foot Drop Guillain-Barre Syndrome Hepatic Adenomas, Familial Hereditary Neuropathies Hereditary Neuropathy with Liability to Pressure Palsy Hypertrophic Neuropathy of Dejerine-Sottas Hypomyelinating Leukodystrophy Hypomyelinating Leukoencephalopathy Ichthyosis Prematurity Syndrome Juvenile Hereditary Hemochromatosis Leukodystrophy Leukodystrophy, Hypomyelinating, 2 Leukodystrophy, Hypomyelinating, 4 Locked-in Syndrome Malaria Mannosidosis, Beta a, Lysosomal Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 Microcephaly Microphthalmia, Syndromic 9 Mitochondrial Dna Depletion Syndrome 4a Mosaic Variegated Aneuploidy Syndrome 1 Motor Peripheral Neuropathy Multiple Sulfatase Deficiency Muscular Atrophy Nervous System Disease Neuritis Neuronitis Neuropathy Neuropathy, Hereditary Sensory and Autonomic, Type Iii Neuropathy, Hereditary, with Liability to Pressure Palsies Niemann-Pick Disease, Type a Optic Neuritis Paraplegia Pelizaeus-Merzbacher Disease, Classic Form Pelizaeus-Merzbacher-Like Disease Peripheral Nervous System Disease Persistent Mullerian Duct Syndrome Persistent Mullerian Duct Syndrome, Types I and Ii Plp1-Related Disorders Polyneuropathy Polyradiculoneuropathy Quadriplegia Sensory Peripheral Neuropathy Spastic Cerebral Palsy Spasticity Spastic Paraplegia 2, X-Linked Spastic Quadriplegia Sphingolipidosis Spinal Muscular Atrophy Tooth Disease Tremor Tuberous Sclerosis Tuberous Sclerosis 1 Tumefactive Multiple Sclerosis