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Query OMIM entry list
182600
SPG3A
SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT
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Neoplasms
Neoplasms by Histologic Type
Neoplasms, Germ Cell and Embryonal
Neuroectodermal Tumors
Neuroendocrine Tumors
Paraganglioma
Neoplasms, Nerve Tissue
Neuroectodermal Tumors
Neuroendocrine Tumors
Paraganglioma
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dysostoses
Synostosis
Syndactyly
Foot Deformities
Foot Deformities, Congenital
Clubfoot
Muscular Diseases
Muscle Spasticity
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Lower Extremity Deformities, Congenital
Foot Deformities, Congenital
Clubfoot
Syndactyly
Synostosis
Syndactyly
Digestive System Diseases
Digestive System Abnormalities
Hirschsprung Disease
Gastrointestinal Diseases
Intestinal Diseases
Colonic Diseases
Megacolon
Hirschsprung Disease
Respiratory Tract Diseases
Respiration Disorders
Apnea
Sleep Apnea Syndromes
Nervous System Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Central Nervous System Diseases
Brain Diseases
Brain Damage, Chronic
Cerebral Palsy
Cerebellar Diseases
Cerebellar Ataxia
Cerebrovascular Disorders
Intracranial Arteriovenous Malformations
Epilepsy
Epilepsies, Partial
Epilepsy, Generalized
Epilepsy, Tonic-Clonic
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Demyelinating Diseases
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Nervous System Malformations
Central Nervous System Vascular Malformations
Intracranial Arteriovenous Malformations
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Hereditary Sensory and Autonomic Neuropathies
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Hereditary Sensory and Autonomic Neuropathies
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Gait Disorders, Neurologic
Neuromuscular Manifestations
Muscle Hypertonia
Muscle Spasticity
Muscular Atrophy
Spasm
Pain
Paralysis
Paraplegia
Urinary Bladder, Neurogenic
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Hereditary Sensory and Autonomic Neuropathies
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Sleep Disorders
Dyssomnias
Sleep Disorders, Intrinsic
Sleep Apnea Syndromes
Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Ocular Motility Disorders
Nystagmus, Pathologic
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Male Urogenital Diseases
Urologic Diseases
Urinary Bladder Diseases
Urinary Bladder, Neurogenic
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Urinary Bladder Diseases
Urinary Bladder, Neurogenic
Cardiovascular Diseases
Cardiovascular Abnormalities
Vascular Malformations
Arteriovenous Malformations
Intracranial Arteriovenous Malformations
Central Nervous System Vascular Malformations
Intracranial Arteriovenous Malformations
Vascular Diseases
Arteriovenous Malformations
Intracranial Arteriovenous Malformations
Cerebrovascular Disorders
Intracranial Arterial Diseases
Intracranial Arteriovenous Malformations
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Cardiovascular Abnormalities
Vascular Malformations
Arteriovenous Malformations
Intracranial Arteriovenous Malformations
Central Nervous System Vascular Malformations
Intracranial Arteriovenous Malformations
Chromosome Disorders
Digestive System Abnormalities
Hirschsprung Disease
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Foot Deformities, Congenital
Clubfoot
Syndactyly
Synostosis
Syndactyly
Nervous System Malformations
Central Nervous System Vascular Malformations
Intracranial Arteriovenous Malformations
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Hereditary Sensory and Autonomic Neuropathies
Genetic Diseases, Inborn
Chromosome Disorders
Eye Diseases, Hereditary
Retinitis Pigmentosa
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Hereditary Sensory and Autonomic Neuropathies
Immune System Diseases
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Chromosome Aberrations
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Anticipation, Genetic
Nerve Degeneration
Wallerian Degeneration
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Gait Disorders, Neurologic
Neuromuscular Manifestations
Muscle Hypertonia
Muscle Spasticity
Muscular Atrophy
Spasm
Pain
Paralysis
Paraplegia
Urinary Bladder, Neurogenic
Pain
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