Autosomal dominant spastic spastic paraplegia hereditary. Medical search. Frequent questions

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Anatomy10

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

Organisms1

Human T-lymphotropic virus 1

Diseases39

Spastic Paraplegia, Hereditary Paraplegia Paraparesis, Spastic Muscle Spasticity Paraparesis, Tropical Spastic Polycystic Kidney, Autosomal Dominant Cerebral Palsy Cerebellar Ataxia Spasm Reflex, Babinski Syndrome Spinocerebellar Degenerations Agenesis of Corpus Callosum Pelizaeus-Merzbacher Disease Quadriplegia Hereditary Sensory and Motor Neuropathy Spinal Cord Ischemia Optic Atrophy Intellectual Disability Equinus Deformity Spinal Cord Injuries Hemiplegia Retinitis Pigmentosa Coronary Vasospasm Sex Chromosome Aberrations Motor Neuron Disease Aortic Aneurysm, Thoracic Tuberculosis, Spinal Optic Atrophies, Hereditary Paraparesis Angina Pectoris, Variant Spinal Cord Compression Optic Atrophy, Autosomal Dominant Reflex, Abnormal Hydrocephalus HTLV-I Infections Disease Models, Animal Paralysis Nerve Degeneration

Chemicals and Drugs14

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

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

Psychiatry and Psychology2

Human Characteristics Intellectual Disability

Phenomena and Processes28

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

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care2

Age of Onset Family Health

Anatomy Organisms 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 Genes, Dominant Muscle Spasticity Pedigree Paraparesis, Tropical Spastic Genes, Recessive Polycystic Kidney, Autosomal Dominant Lod Score Cerebral Palsy Adaptor Protein Complex 4 Mutation Cerebellar Ataxia Genetic Linkage Mutation, Missense Adenosine Triphosphatases Spasm Chromosomes, Human, Pair 2 Phenotype DNA Mutational Analysis Reflex, Babinski Syndrome Age of Onset Genetic Heterogeneity Chromosome Mapping Spinocerebellar Degenerations Agenesis of Corpus Callosum Pelizaeus-Merzbacher Disease Quadriplegia Hereditary Sensory and Motor Neuropathy Heterozygote Spinal Cord Ischemia Optic Atrophy Exome Human Characteristics Consanguinity Intellectual Disability Spinal Cord Haplotypes Equinus Deformity Molecular Sequence Data Leukocyte L1 Antigen Complex GTP Phosphohydrolases Motor Neurons TRPP Cation Channels Spinal Cord Injuries ATP-Dependent Proteases Exons Hemiplegia Myelin Proteolipid Protein Corpus Callosum Genetic Markers Retinitis Pigmentosa Coronary Vasospasm Codon, Nonsense Metalloendopeptidases Axons Family Health Sex Chromosome Aberrations Motor Neuron Disease Aortic Aneurysm, Thoracic Magnetic Resonance Imaging Base Sequence Tuberculosis, Spinal Human T-lymphotropic virus 1 Optic Atrophies, Hereditary Genotype Microtubules Paraparesis Angina Pectoris, Variant Point Mutation Spinal Cord Compression Optic Atrophy, Autosomal Dominant Membrane Proteins X Chromosome Homozygote Chromosomes, Human, Pair 14 Neural Conduction Reflex, Abnormal Chromosomes, Human, Pair 15 Hydrocephalus HTLV-I Infections Neuromuscular Agents Botulinum Toxins, Type A Laminectomy Brain Gait Disease Models, Animal Amino Acid Sequence Proteins Paralysis Nerve Degeneration

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