Autosomal dominant neuropathy. Medical search. Frequent questions

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Anatomy39

Sural Nerve Peripheral Nerves Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 16 Sciatic Nerve Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 12 Nerve Fibers Axons Ulnar Nerve Chromosomes, Human, Pair 7 Toes Kidney Fundus Oculi Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 5 Optic Nerve Chromosomes, Human, Pair 3 Cell Line Peroneal Nerve Peripheral Nervous System Schwann Cells Chromosomes, Human, Pair 10 Skin Cells, Cultured Median Nerve Tibial Nerve Chromosomes, Human, Pair 11 Vasa Nervorum Chromosomes, Human, Pair 9 Motor Neurons Chromosomes, Human, Pair 20 Ganglia, Spinal Foot Myelin Sheath Cyst Fluid

Organisms1

Mice, Transgenic

Diseases125

Diabetic Neuropathies Polycystic Kidney, Autosomal Dominant Peripheral Nervous System Diseases Hereditary Sensory and Motor Neuropathy Hereditary Sensory and Autonomic Neuropathies Optic Neuropathy, Ischemic Charcot-Marie-Tooth Disease Retinitis Pigmentosa Optic Atrophy, Autosomal Dominant Polyneuropathies Ulnar Neuropathies Syndrome Autonomic Nervous System Diseases Alcoholic Neuropathy Cataract Polycystic Kidney Diseases CADASIL Cerebellar Ataxia Femoral Neuropathy Optic Atrophy, Hereditary, Leber Spinocerebellar Degenerations Optic Atrophies, Hereditary Spastic Paraplegia, Hereditary Optic Nerve Diseases Median Neuropathy Dementia, Multi-Infarct Amyloid Neuropathies Hearing Loss, Sensorineural Chromosome Disorders Hand Deformities, Congenital Cysts Cranial Nerve Diseases Abnormalities, Multiple Nervous System Diseases Ulnar Nerve Compression Syndromes Foot Deformities, Congenital Spinocerebellar Ataxias Nails, Malformed Optic Atrophy Demyelinating Diseases Disease Models, Animal Amyloid Neuropathies, Familial Ectodermal Dysplasia Tuberous Sclerosis Keratoderma, Palmoplantar Muscular Diseases Motor Neuron Disease Skin Diseases, Genetic Eye Diseases, Hereditary Deafness Peroneal Neuropathies Neuromuscular Diseases Syndactyly Genetic Predisposition to Disease Paresthesia Neurofibromatosis 1 Sensation Disorders Epilepsy, Frontal Lobe Ophthalmoplegia Telangiectasia, Hereditary Hemorrhagic Hearing Loss, Central Nerve Compression Syndromes Mandibulofacial Dysostosis Reflex, Abnormal Ataxia Polyradiculoneuropathy Exostoses, Multiple Hereditary Bone Diseases, Developmental Arthrogryposis Tooth Abnormalities Tibial Neuropathy Paraneoplastic Polyneuropathy Ophthalmoplegia, Chronic Progressive External Retinal Degeneration Neuralgia Vestibulocochlear Nerve Diseases Noonan Syndrome Sciatic Neuropathy Guillain-Barre Syndrome Genetic Diseases, Inborn Disease Progression Job Syndrome Brachial Plexus Neuritis Pigmentation Disorders Diabetic Foot Dystonia Porphyrias, Hepatic Epilepsy, Partial, Sensory Blepharoptosis Diabetes Insipidus, Neurogenic Chorea Marfan Syndrome Anticipation, Genetic Osteochondrodysplasias Dystonia Musculorum Deformans Brachial Plexus Neuropathies Nail-Patella Syndrome Nerve Degeneration Eye Abnormalities Hearing Loss Branchio-Oto-Renal Syndrome Hypohidrosis Neuritis Muscle Weakness Polydactyly Foot Ulcer Darier Disease Corneal Dystrophies, Hereditary Cleidocranial Dysplasia Hypotrichosis Muscular Dystrophies Muscular Dystrophy, Emery-Dreifuss Hypesthesia Mononeuropathies Hoarseness Hypoparathyroidism Kidney Diseases, Cystic Neurotoxicity Syndromes Diabetes Mellitus, Experimental Coloboma Diabetes Mellitus, Type 2 Diabetes Mellitus, Type 1 Genetic Diseases, X-Linked Machado-Joseph Disease Limb Deformities, Congenital

Chemicals and Drugs26

TRPP Cation Channels Genetic Markers Eye Proteins gamma-Crystallins beta-Crystallin A Chain Codon, Nonsense Rhodopsin Peripherins Membrane Proteins Myelin P0 Protein DNA, Mitochondrial beta-Crystallin B Chain GTP Phosphohydrolases Myelin Proteins Nerve Tissue Proteins Connexins Proteins DNA Primers DNA Neurophysins Guanylate Cyclase-Activating Proteins Mutant Proteins Dynamin II RNA, Messenger RNA Splice Sites Prealbumin

Analytical, Diagnostic and Therapeutic Techniques and Equipment21

Pedigree DNA Mutational Analysis Chromosome Mapping Electroretinography Polymerase Chain Reaction Electrodiagnosis Genetic Testing Disease Models, Animal Amino Acid Substitution Diagnostic Techniques, Neurological Sequence Analysis, DNA Neurologic Examination Electromyography Reflex, Abnormal Magnetic Resonance Imaging Biopsy Visual Acuity Transfection Case-Control Studies Diabetes Mellitus, Experimental Blotting, Western

Psychiatry and Psychology6

Dementia, Multi-Infarct Family Visual Acuity Visual Fields Sensation Sensory Thresholds

Phenomena and Processes59

Genes, Dominant Genetic Linkage Mutation Lod Score Neural Conduction Mutation, Missense Phenotype Haplotypes Penetrance Genes, Recessive Heterozygote Genetic Heterogeneity Genetic Markers Base Sequence Exons Genotype Chromosomes, Human, Pair 2 Frameshift Mutation Point Mutation Microsatellite Repeats Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 19 Codon, Nonsense Chromosomes, Human, Pair 1 Alleles Polymorphism, Single-Stranded Conformational Amino Acid Substitution Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 4 Genetic Predisposition to Disease Amino Acid Sequence Chromosomes, Human, Pair 12 Homozygote Chromosomes, Human, Pair 7 Polymorphism, Genetic Reflex, Abnormal Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 3 Exome Founder Effect Sequence Deletion Consanguinity Time Factors Polymorphism, Restriction Fragment Length Anticipation, Genetic Visual Acuity Germ-Line Mutation Visual Fields Chromosomes, Human, Pair 10 Transfection Sensation Chromosomes, Human, Pair 11 Signal Transduction Gene Deletion Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 20 Protein Structure, Tertiary RNA Splice Sites

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups1

Asian Continental Ancestry Group

Health Care5

Age of Onset Family Health Genetic Testing Case-Control Studies Genetic Counseling

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care

Genes, Dominant Diabetic Neuropathies Polycystic Kidney, Autosomal Dominant Pedigree Peripheral Nervous System Diseases Hereditary Sensory and Motor Neuropathy Hereditary Sensory and Autonomic Neuropathies Genetic Linkage Mutation Lod Score TRPP Cation Channels Optic Neuropathy, Ischemic Charcot-Marie-Tooth Disease Sural Nerve Retinitis Pigmentosa Optic Atrophy, Autosomal Dominant Polyneuropathies DNA Mutational Analysis Neural Conduction Mutation, Missense Phenotype Ulnar Neuropathies Chromosome Mapping Syndrome Autonomic Nervous System Diseases Alcoholic Neuropathy Cataract Polycystic Kidney Diseases CADASIL Molecular Sequence Data Haplotypes Penetrance Cerebellar Ataxia Genes, Recessive Heterozygote Age of Onset Femoral Neuropathy Genetic Heterogeneity Optic Atrophy, Hereditary, Leber Genetic Markers Spinocerebellar Degenerations Optic Atrophies, Hereditary Family Health Spastic Paraplegia, Hereditary Optic Nerve Diseases Median Neuropathy Dementia, Multi-Infarct Base Sequence Peripheral Nerves Exons Amyloid Neuropathies Eye Proteins Hearing Loss, Sensorineural Genotype Chromosomes, Human, Pair 2 Chromosome Disorders Frameshift Mutation Hand Deformities, Congenital Point Mutation Microsatellite Repeats Chromosomes, Human, Pair 16 Cysts Sciatic Nerve Cranial Nerve Diseases Abnormalities, Multiple Electroretinography gamma-Crystallins Nervous System Diseases Ulnar Nerve Compression Syndromes Foot Deformities, Congenital Chromosomes, Human, Pair 19 Spinocerebellar Ataxias Nails, Malformed Polymerase Chain Reaction Electrodiagnosis beta-Crystallin A Chain Codon, Nonsense Optic Atrophy Chromosomes, Human, Pair 1 Alleles Genetic Testing Demyelinating Diseases Polymorphism, Single-Stranded Conformational Disease Models, Animal Rhodopsin Amyloid Neuropathies, Familial Amino Acid Substitution Ectodermal Dysplasia Diagnostic Techniques, Neurological Tuberous Sclerosis Keratoderma, Palmoplantar Muscular Diseases Motor Neuron Disease Chromosomes, Human, Pair 17 Skin Diseases, Genetic Eye Diseases, Hereditary Deafness Peroneal Neuropathies Sequence Analysis, DNA Chromosomes, Human, Pair 4

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