Genetic study 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 15 Chromosomes, Human, Pair 14

Diseases28

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

Chemicals and Drugs11

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment6

Pedigree Reflex, Babinski Chromosome Mapping DNA Mutational Analysis Magnetic Resonance Imaging Laminectomy

Psychiatry and Psychology2

Human Characteristics Intellectual Disability

Phenomena and Processes22

Genes, Recessive Genes, Dominant Lod Score Mutation Phenotype Mutation, Missense Chromosomes, Human, Pair 2 Genetic Linkage Genetic Heterogeneity Exome Consanguinity Heterozygote Sex Chromosome Aberrations Haplotypes Genotype Genetic Markers X Chromosome Neural Conduction Chromosomes, Human, Pair 15 Exons Codon, Nonsense Chromosomes, Human, Pair 14

Information Science1

Molecular Sequence Data

Health Care2

Age of Onset Family Health

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

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