Informaţii despre

Nume Neuropathy, Congenital Hypomyelinating or Amyelinating, Autosomal Recessive
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Hereditary motor and sensory neuropathy
Clasificare anatomică Malacards Boli neuronale

Vezi şi

Boli A-Z 46,xy Sex Reversal 2 Adie Pupil Agenesis of the Corpus Callosum with Peripheral Neuropathy Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amyotrophic Neuralgia Angel-Shaped Phalangoepiphyseal Dysplasia Aniridia 1 Anorexia Nervosa 1 Aplasia Cutis Congenita Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autism Axonal Neuropathy Blood Group--Ahonen Blood Group, I System Brachial Plexus Neuropathy Cauda Equina Syndrome Centronuclear Myopathy Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease and Deafness Charcot-Marie-Tooth Disease, Axonal, Type 2a1 Charcot-Marie-Tooth Disease, Axonal, Type 2b Charcot-Marie-Tooth Disease, Axonal, Type 2e Charcot-Marie-Tooth Disease, Axonal, Type 2f Charcot-Marie-Tooth Disease, Axonal, Type 2i Charcot-Marie-Tooth Disease, Axonal, Type 2j Charcot-Marie-Tooth Disease, Axonal, Type 2k Charcot-Marie-Tooth Disease, Axonal, Type 2l Charcot-Marie-Tooth Disease, Demyelinating, Type 1a Charcot-Marie-Tooth Disease, Demyelinating, Type 1b Charcot-Marie-Tooth Disease, Demyelinating, Type 1c Charcot-Marie-Tooth Disease, Demyelinating, Type 1d Charcot-Marie-Tooth Disease, Demyelinating, Type 1f Charcot-Marie-Tooth Disease, Demyelinating, Type 4f Charcot-Marie-Tooth Disease, Dominant Intermediate a Charcot-Marie-Tooth Disease, Dominant Intermediate B Charcot-Marie-Tooth Disease Type 2a Charcot-Marie-Tooth Disease Type 2k Charcot-Marie-Tooth Disease, Type 4a Charcot-Marie-Tooth Disease, Type 4b1 Charcot-Marie-Tooth Disease, Type 4b2 Charcot-Marie-Tooth Disease, Type 4b3 Charcot-Marie-Tooth Disease, Type 4c Charcot-Marie-Tooth Disease, Type 4d Charcot-Marie-Tooth Disease, Type 4h Charcot-Marie-Tooth Disease, Type 4j Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 Charcot-Marie-Tooth Disease, X-Linked Recessive, 2 Charcot-Marie-Tooth Disease, X-Linked Recessive, 3 Charcot-Marie-Tooth Neuropathy Type 1 Charcot-Marie-Tooth Neuropathy Type 2a Charcot-Marie-Tooth Neuropathy Type 4j Chronic Inflammatory Demyelinating Polyneuropathy Congenital Hypomyelination Neuropathy Demyelinating Polyneuropathy Early-Onset Glaucoma Foot Drop Glaucoma, Hereditary Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency Gonadal Dysgenesis Hepatic Adenomas, Familial Hereditary Motor and Sensory Neuropathy, Type Iic Hereditary Neuropathies Hereditary Neuropathy with Liability to Pressure Palsy Hereditary Sensory Neuropathy Hereditary Spastic Paraplegia Hypertrophic Neuropathy of Dejerine-Sottas Hypotonia Juvenile Glaucoma Lambert-Eaton Myasthenic Syndrome Laryngeal Cleft Motor Peripheral Neuropathy Multiple Sclerosis Myopathy, Centronuclear, X-Linked Myotonic Dystrophy Neuromuscular Disease Neuronitis Neuropathy Neuropathy, Hereditary Motor and Sensory, Russe Type Neuropathy, Hereditary Motor and Sensory, Type Via Neuropathy, Hereditary, with Liability to Pressure Palsies Paraplegia Peripheral Nervous System Disease Polykaryocytosis Inducer Polyneuropathy Pseudomyxoma Peritonei Roussy-Levy Hereditary Areflexic Dystasia Sensory Neuropathy Type 1 Sensory Peripheral Neuropathy Slowed Nerve Conduction Velocity, Autosomal Dominant Spasticity Superior Mesenteric Artery Syndrome Tetraamelia Syndrome, Autosomal Recessive Tooth Disease Toxic Oil Syndrome Yunis-Varon Syndrome