Inherited diseases 1983 spastic paraplegia hereditary. Medical search. Frequent questions

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Anatomy9

Chromosomes, Human, Pair 2 Spinal Cord Corpus Callosum Motor Neurons Axons Microtubules X Chromosome Chromosomes, Human, Pair 14 Chromosomes, Human, Pair 15

Diseases32

Spastic Paraplegia, Hereditary Paraplegia Paraparesis, Spastic Genetic Diseases, Inborn Muscle Spasticity Paraparesis, Tropical Spastic Cerebellar Ataxia Reflex, Babinski Agenesis of Corpus Callosum Syndrome Spasm Spinal Cord Ischemia Pelizaeus-Merzbacher Disease Cerebral Palsy Hereditary Sensory and Motor Neuropathy Quadriplegia Optic Atrophy Spinocerebellar Degenerations Intellectual Disability Spinal Cord Injuries Tuberculosis, Spinal Paraparesis Aortic Aneurysm, Thoracic Sex Chromosome Aberrations Disease Models, Animal Spinal Cord Compression Motor Neuron Disease Optic Atrophies, Hereditary Cystic Fibrosis Hydrocephalus Equinus Deformity Genetic Predisposition to Disease

Chemicals and Drugs12

Adaptor Protein Complex 4 Adenosine Triphosphatases Codon, Nonsense Leukocyte L1 Antigen Complex ATP-Dependent Proteases Myelin Proteolipid Protein Ferrochelatase Metalloendopeptidases Membrane Proteins GTP Phosphohydrolases Genetic Markers Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

Pedigree Reflex, Babinski Chromosome Mapping DNA Mutational Analysis Disease Models, Animal Laminectomy Genetic Therapy Magnetic Resonance Imaging Genetic Testing

Psychiatry and Psychology2

Human Characteristics Intellectual Disability

Phenomena and Processes28

Mutation Mutation, Missense Genes, Recessive Genes, Dominant Genetic Linkage Phenotype Lod Score Heterozygote Chromosomes, Human, Pair 2 Codon, Nonsense Genetic Heterogeneity Exons Exome Point Mutation Heredity Consanguinity Base Sequence Genotype Sex Chromosome Aberrations Amino Acid Sequence Genetic Markers X Chromosome Neural Conduction Haplotypes Chromosomes, Human, Pair 14 Genetic Predisposition to Disease Chromosomes, Human, Pair 15 Genome, Human

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care3

Age of Onset Family Health Genetic Testing

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Information Science Health Care

Spastic Paraplegia, Hereditary Paraplegia Paraparesis, Spastic Pedigree Genetic Diseases, Inborn Muscle Spasticity Mutation Mutation, Missense Adaptor Protein Complex 4 Genes, Recessive Genes, Dominant Adenosine Triphosphatases Paraparesis, Tropical Spastic Genetic Linkage Phenotype Cerebellar Ataxia Reflex, Babinski Agenesis of Corpus Callosum Syndrome Spasm Lod Score Chromosome Mapping DNA Mutational Analysis Spinal Cord Ischemia Heterozygote Pelizaeus-Merzbacher Disease Chromosomes, Human, Pair 2 Codon, Nonsense Cerebral Palsy Human Characteristics Hereditary Sensory and Motor Neuropathy Quadriplegia Optic Atrophy Age of Onset Genetic Heterogeneity Exons Exome Spinal Cord Molecular Sequence Data Leukocyte L1 Antigen Complex Point Mutation Heredity Spinocerebellar Degenerations Intellectual Disability Consanguinity Spinal Cord Injuries ATP-Dependent Proteases Myelin Proteolipid Protein Corpus Callosum Base Sequence Motor Neurons Family Health Ferrochelatase Metalloendopeptidases Tuberculosis, Spinal Membrane Proteins Genotype GTP Phosphohydrolases Paraparesis Aortic Aneurysm, Thoracic Axons Sex Chromosome Aberrations Disease Models, Animal Amino Acid Sequence Genetic Markers Microtubules Spinal Cord Compression Motor Neuron Disease Optic Atrophies, Hereditary Proteins Cystic Fibrosis Hydrocephalus Laminectomy Genetic Therapy Magnetic Resonance Imaging X Chromosome Neural Conduction Haplotypes Chromosomes, Human, Pair 14 Equinus Deformity Genetic Testing Genetic Predisposition to Disease Chromosomes, Human, Pair 15 Genome, Human

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