Autosomal recessive 1983 spastic paraplegia hereditary. Medical search. Frequent questions

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Anatomy11

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

Diseases37

Spastic Paraplegia, Hereditary Paraplegia Paraparesis, Spastic Muscle Spasticity Cerebellar Ataxia Syndrome Paraparesis, Tropical Spastic Agenesis of Corpus Callosum Reflex, Babinski Intellectual Disability Spasm Polycystic Kidney, Autosomal Recessive Optic Atrophy Pelizaeus-Merzbacher Disease Spinal Cord Ischemia Hereditary Sensory and Motor Neuropathy Cerebral Palsy Spinocerebellar Degenerations Quadriplegia Sex Chromosome Aberrations Spinal Cord Injuries Retinitis Pigmentosa Microcephaly Abnormalities, Multiple Tuberculosis, Spinal Optic Atrophies, Hereditary Paraparesis Aortic Aneurysm, Thoracic Motor Neuron Disease Ichthyosis Spinal Cord Compression Hydrocephalus Hypotrichosis Disease Models, Animal Ichthyosiform Erythroderma, Congenital Nerve Degeneration Equinus Deformity

Chemicals and Drugs12

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment8

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

Psychiatry and Psychology2

Intellectual Disability Human Characteristics

Phenomena and Processes27

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

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

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