Charcot-Marie-Tooth Disease Type 4E
Charcot-Marie-Tooth Disease Type 4E
About the Disease
Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive, also known as charcot-marie-tooth disease type 4e, is related to charcot-marie-tooth disease, demyelinating, type 1b and charcot-marie-tooth disease, demyelinating, type 1a. An important gene associated with Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive is EGR2 (Early Growth Response 2), and among its related pathways/superpathways are PI Metabolism and Neural crest differentiation. The drugs Ascorbic acid and Micronutrients have been mentioned in the context of this disorder. Affiliated tissues include Peripheral Nervous System, dorsal root ganglion and spinal cord, and related phenotypes are respiratory insufficiency and neonatal hypotonia
Common Targets
PMP22 | CNTNAP1
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Vascular Cognitive Impairment | Alexander Disease | Eczema | Methylmalonic Aciduria And Homocystinuria, CblC Type | McCune-Albright Syndrome | Hypersomnia | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Malaria, Cerebral | Cyst | Kaposi Sarcoma | Blastoma, Pleuropulmonary | Schamberg Disease | Carcinoma, Signet Ring Cell | Pulmonary Vein Stenosis | Homocystinuria | Sleep Apnea, Central | Hereditary Neuropathy With Liability To Pressure Palsies | Learning Disability | Hyperkalemic Periodic Paralysis | Rubeosis Iridis | Vitelliform Macular Dystrophy | Acrodermatitis | Dysfibrinogenemia | Spinocerebellar Ataxia Type 31 | Osteopathia Striata With Cranial Sclerosis | Zygomycosis | Schistosomiasis | Microcephaly, Seizures, And Developmental Delay | Diabetic Encephalopathy | Molybdenum Cofactor Deficiency | Congenital Hereditary Endothelial Dystrophy Type II | Tularemia | Iron Deficiency Anemia | Vitreoretinopathy, Proliferative | Chronic Granulomatous Disease, X-linked | Nephroblastoma | Toxic Epidermal Necrolysis | Epidermolytic Ichthyosis, Annular | Spinocerebellar Ataxia Type 20 | Rhinitis | Hereditary Elliptocytosis | Kashin-Beck Disease | Analgesia | Birt-Hogg-Dube Syndrome | Relapsing Polychondritis | Giant Cell Arteritis | Thrombasthenia | Congenital Afibrinogenemia | Rheumatoid Arthritis | Pseudo-pseudohypoparathyroidism | Myoclonic Atonic Epilepsy | Lennox-Gastaut Syndrome | Carbohydrate Metabolism Disorders | Infantile Neuroaxonal Dystrophy | Endometritis | Thanatophoric Dysplasia | Pleurisy | Wolman Disease | Coma | Jaundice, Obstructive | Pseudohypoparathyroidism Type 1B | Adenosine Deaminase Deficiency | Mannosidase Deficiency Diseases | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Myasthenia | Orotic Aciduria | Myeloid Leukemia | Waardenburg Syndrome Type 2 | Postpartum Depression | Avian Influenza | Congestive Heart Failure | Presbyopia | HELLP Syndrome | Gray Platelet Syndrome | Oligoastrocytoma | Hereditary Spastic Paraplegia | Oculocutaneous Albinism | Bronchiectasis | Keratitis | Myoclonic Epilepsy With Ragged Red Fibers | Focal Segmental Glomerulosclerosis | DNA Ligase IV Deficiency | Premature Ejaculation | Riboflavin Transporter Deficiency Neuronopathy | Episodic Ataxia Type 2 | Saethre-Chotzen Syndrome | Meningioma, Benign | Spinocerebellar Ataxia Type 14 | Hypertension | Osteosarcoma | Von Hippel-Lindau Disease | Myocarditis | Cabezas Syndrome | Wilson's Disease | FG Syndrome | Smith-Magenis Syndrome | Microphthalmia, Syndromic 7 | Chronic Enteropathy Associated With SLCO2A1 Gene | Cenani-Lenz Syndactyly Syndrome | Kindler Syndrome | Neurofibromatosis | L-2-Hydroxyglutaric Aciduria | Pre-eclampsia | Camurati-Engelmann Disease | Asthma, Nocturnal | Adult Polyglucosan Body Disease | Scapuloperoneal Spinal Muscular Atrophy | Obesity | Inflammatory Joint Disease | 5-oxoprolinase Deficiency | Choroideremia | Seminoma | Leprosy | Intermittent Claudication | Ligneous Conjunctivitis | Dyslipidemia | Spinal Muscular Atrophy 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| Retinal Detachment | Crohn's Disease | Microcephaly | Congenital Ichthyosiform Erythroderma | Saul-Wilson Syndrome | Familial Mediterranean Fever | Asperger Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Intermittent Explosive Disorder | Shprintzen-Goldberg Syndrome | Spondyloperipheral Dysplasia | Charcot-Marie-Tooth Disease, Type 6 | Hyper IgE Syndrome | Asthma | Poikiloderma With Neutropenia | Congenital Torticollis | Fabry's Disease | Leukodystrophies | Christianson Syndrome | Eating Disorder | Sleep Apnea | Marfan Syndrome | Alveolar Capillary Dysplasia | Renal Oncocytoma | Dysgerminoma | Stuve-Wiedemann Syndrome | Echinococcosis | Alopecia | Dyslexia | Megalencephaly | Anorectal Fistula | Colitis, Collagenous | Multiple Sclerosis, Chronic Progressive | Pyruvate Dehydrogenase Deficiency | Epidermolysis Bullosa Simplex | Spondyloarthritis | Familial Cerebral Amyloid Angiopathy | Cherubism | Malignant Fibrous Histiocytoma | Leukocyte Adhesion Deficiency | Xeroderma 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Acute Tubular Necrosis | Early Infantile Epileptic Encephalopathy 1 | Polycythemia | Early Infantile Epileptic Encephalopathy 28 | Brachydactyly | Prostatitis | Bernard-Soulier Syndrome | AIDS Dementia Complex | Hyperostosis | Granuloma Annulare | Osteogenesis Imperfecta Type II | Arthritis, Psoriatic | Aicardi-Goutieres Syndrome | Hartsfield Syndrome | Diamond-Blackfan Anemia | Vaginitis | Neurofibromatosis Type 1 | Multiple Sclerosis, Secondary Progressive | Hypokalemic Periodic Paralysis | NGLY1 Deficiency | Wolfram Syndrome 2 | Hypohidrotic Ectodermal Dysplasia, X-linked | Optic Nerve Diseases | Cancer, Colon | Myopathy | Light Chain Amyloidosis | NDH Syndrome | Cri-du-chat Syndrome | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Malnutrition | Hereditary Sensory And Autonomic Neuropathy | Cardiac Arrest | Smoldering Myeloma | Usher Syndrome Type IIC | Spina Bifida | Sickle Cell Anemia | Liver Failure, Acute Infantile | Hepatitis | Micropenis | X-linked 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