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Charcot-Marie-Tooth Disease
Informaţii despre
Nume
Charcot-Marie-Tooth Disease
Pagina Web
www.malacards.org
Clasificare globală Malacards
Boli genetice
;
Boli metabolice
;
Boli rare
Clasificari ICD10
Hereditary motor and sensory neuropathy
Clasificare anatomică Malacards
Boli musculare
;
Boli neuronale
Boli din aceeaşi familie
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due to Dgat2 Mutation
;
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due to Kif5a Mutation
;
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due to Tfg Mutation
;
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2g
;
Autosomal Dominant Intermediate Charcot-Marie-Tooth
;
Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease Type B
;
Autosomal Recessive Intermediate Charcot-Marie-Tooth Disease
;
Charcot-Marie-Tooth Disease Intermediate Type
;
Charcot-Marie-Tooth Disease Type 2a
;
Charcot-Marie-Tooth Disease Type 2a2
;
Charcot-Marie-Tooth Disease Type 2c
;
Charcot-Marie-Tooth Disease Type 2f
;
Charcot-Marie-Tooth Disease Type 2g
;
Charcot-Marie-Tooth Disease Type 2k
;
Charcot-Marie-Tooth Disease Type 2l
;
Charcot-Marie-Tooth Disease Type 2n
;
Charcot-Marie-Tooth Disease Type 2o
;
Charcot-Marie-Tooth Disease Type 2q
;
Charcot-Marie-Tooth Disease Type 5
;
Charcot-Marie-Tooth Disease Type 7
;
Charcot-Marie-Tooth Disease, Dominant Intermediate a
;
Charcot-Marie-Tooth Disease, Dominant Intermediate B
;
Charcot-Marie-Tooth Disease, Dominant Intermediate C
;
Charcot-Marie-Tooth Disease, Recessive Intermediate a
;
Charcot-Marie-Tooth Disease, Recessive Intermediate B
;
Charcot-Marie-Tooth Disease, Recessive Intermediate C
;
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, Type 4k
Vezi şi
Boli A-Z
Acute Disseminated Encephalomyelitis
Aging
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome
Alport Syndrome, X-Linked
Al-Raqad Syndrome
Amyloidosis
Amyotrophic Lateral Sclerosis Type 5
Amyotrophic Neuralgia
Androgen Insensitivity Syndrome, Mild
Aniridia 1
Anorexia Nervosa 1
Antisynthetase Syndrome
Arthrochalasia Ehlers-Danlos Syndrome
Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect
Arts Syndrome
Ataxia and Polyneuropathy, Adult-Onset
Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus
Autonomic Dysfunction
Autonomic Neuropathy
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2g
Autosomal Dominant Intermediate Charcot-Marie-Tooth
Autosomal Recessive Intermediate Charcot-Marie-Tooth Disease
Axonal Neuropathy
Baraitser-Winter Syndrome 1
Blood Group--Ahonen
Blood Group, Dombrock System
Blood Group, I System
Cataract
Cauda Equina Syndrome
Centronuclear Myopathy
Cerebritis
Cervicitis
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 2b1
Charcot-Marie-Tooth Disease, Axonal, Type 2b2
Charcot-Marie-Tooth Disease, Axonal, Type 2d
Charcot-Marie-Tooth Disease, Axonal, Type 2e
Charcot-Marie-Tooth Disease, Axonal, Type 2f
Charcot-Marie-Tooth Disease, Axonal, Type 2h
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, Axonal, Type 2n
Charcot-Marie-Tooth Disease, Axonal, Type 2p
Charcot-Marie-Tooth Disease, Axonal, Type 2r
Charcot-Marie-Tooth Disease, Axonal, Type 2t
Charcot-Marie-Tooth Disease, Axonal, Type 2u
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 Intermediate Type
Charcot-Marie-Tooth Disease, Recessive Intermediate D
Charcot-Marie-Tooth Disease Type 2a
Charcot-Marie-Tooth Disease Type 2a2
Charcot-Marie-Tooth Disease Type 2c
Charcot-Marie-Tooth Disease Type 2g
Charcot-Marie-Tooth Disease Type 2k
Charcot-Marie-Tooth Disease Type 2l
Charcot-Marie-Tooth Disease Type 2n
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 Dominant, 6
Charcot-Marie-Tooth Hereditary Neuropathy
Charcot-Marie-Tooth Neuropathy Type 1
Charcot-Marie-Tooth Neuropathy Type 2a
Charcot-Marie-Tooth Neuropathy Type 4j
Chromosomal Triplication
Chromosome 17p Duplication
Chronic Inflammatory Demyelinating Polyneuropathy
Cone-Rod Dystrophy 2
Congenital Hypomyelination Neuropathy
Cowchock Syndrome
Crouzon Syndrome with Acanthosis Nigricans
Cutis Verticis Gyrata
Delusional Disorder
Demyelinating Disease
Demyelinating Polyneuropathy
Dermatomyositis
Distal Hereditary Motor Neuropathies
Distal Hereditary Motor Neuropathy, Type V
Dnajb2-Related Charcot-Marie-Tooth Disease Type 2
Early-Onset Glaucoma
Ehlers-Danlos Syndrome
Epilepsy
Epithelial Recurrent Erosion Dystrophy
Erythermalgia, Primary
Ewing Sarcoma
Familial Periodic Paralysis
Fanconi Anemia, Complementation Group E
Floating-Harbor Syndrome
Focal Segmental Glomerulosclerosis
Foot Drop
Glioma
Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency
Guillain-Barre Syndrome
Hantavirus Pulmonary Syndrome
Hellp Syndrome
Hemophilia
Hemophilia a
Hereditary Motor and Sensory Neuropathy, Type Iic
Hereditary Neuropathies
Hereditary Neuropathy with Liability to Pressure Palsy
Hereditary Sensory Neuropathy
Hereditary Spastic Paraplegia
Hypertelorism
Hypertrophic Neuropathy of Dejerine-Sottas
Hypokalemic Periodic Paralysis, Type 1
Hypomelanotic Disorder
Juvenile Spinal Muscular Atrophy
Laryngeal Cleft
Laryngitis
Lateral Sclerosis
Leber Optic Atrophy
Legius Syndrome
Leiomyomatosis
Leukemia
Lymphoblastic Leukemia
Medulloblastoma
Melanoma
Mitochondrial Complex I Deficiency
Mitochondrial Trifunctional Protein Deficiency
Mixed Glioma
Mononeuropathy
Motor Neuron Disease
Motor Peripheral Neuropathy
Multiple Sclerosis
Muscular Atrophy
Muscular Dystrophy
Myasthenia Gravis
Myopathy
Myopathy, Centronuclear, X-Linked
Myotonia
Myotonia Congenita
Narcolepsy
Neuritis
Neurofibroma
Neurofibromatosis, Type Iv, of Riccardi
Neuromuscular Disease
Neuronitis
Neuronopathy, Distal Hereditary Motor, Type Va
Neuropathy
Neuropathy, Congenital Hypomyelinating or Amyelinating, Autosomal Recessive
Neuropathy, Hereditary Motor and Sensory, Russe Type
Neuropathy, Hereditary Motor and Sensory, Type Via
Neuropathy, Hereditary Motor and Sensory, with Deafness, Mental Retardation, and Absent Sensory Large Myelinated Fibers
Neuropathy, Hereditary, with Liability to Pressure Palsies
Niemann-Pick Disease, Type a
Optic Neuritis
Papular Elastorrhexis
Paraplegia
Pelizaeus-Merzbacher Disease
Peripheral Nervous System Disease
Pitt-Hopkins Syndrome
Polymyositis
Polyneuropathy
Polyneuropathy Associated with Igm Monoclonal Gammapathy with Anti-Mag
Polyradiculoneuropathy
Primary Cerebellar Degeneration
Primary Optic Atrophy
Progressive Muscular Atrophy
Pseudomyotonia
Purpura
Relapsing-Remitting Multiple Sclerosis
Restless Legs Syndrome
Riboflavin Transporter Deficiency
Roussy-Levy Hereditary Areflexic Dystasia
Sarcoma
Scoliosis
Seizures, Benign Familial Neonatal, 1
Sensorineural Hearing Loss
Sensory Peripheral Neuropathy
Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis
Sleep Apnea
Sleep Disorder
Spastic Ataxia, Charlevoix-Saguenay Type
Spasticity
Spastic Paraplegia 46, Autosomal Recessive
Spastic Paraplegia 55, Autosomal Recessive
Spastic Paraplegia 57, Autosomal Recessive
Spinal Muscular Atrophy
Spinocerebellar Degeneration
Spondyloocular Syndrome
Superior Mesenteric Artery Syndrome
Thrombotic Thrombocytopenic Purpura
Tooth Disease
Tremor
Trigeminal Neuralgia
Vertical Talus, Congenital
Wallerian Degeneration
X-Linked Charcot-Marie-Tooth Disease
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