Autosomal dominant spastic paraplegia hereditary. Medical search. Frequent questions

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Anatomy12

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

Diseases35

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

Chemicals and Drugs12

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment7

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

Psychiatry and Psychology2

Human Characteristics Intellectual Disability

Phenomena and Processes26

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

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

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

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