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160900
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DYSTROPHIA MYOTONICA 1
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Neoplasms
Neoplasms by Histologic Type
Neoplasms, Nerve Tissue
Nerve Sheath Neoplasms
Neurofibroma
Neurofibromatoses
Neurofibromatosis 1
Neoplastic Syndromes, Hereditary
Neurofibromatoses
Neurofibromatosis 1
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Achondroplasia
Marfan Syndrome
Osteochondrodysplasias
Achondroplasia
Foot Deformities
Foot Deformities, Congenital
Clubfoot
Jaw Diseases
Mandibular Diseases
Craniomandibular Disorders
Temporomandibular Joint Disorders
Joint Diseases
Temporomandibular Joint Disorders
Muscular Diseases
Craniomandibular Disorders
Temporomandibular Joint Disorders
Muscle Weakness
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Myotonic Disorders
Myotonia Congenita
Myotonic Dystrophy
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Lower Extremity Deformities, Congenital
Foot Deformities, Congenital
Clubfoot
Digestive System Diseases
Gastrointestinal Diseases
Esophageal Diseases
Deglutition Disorders
Gastroenteritis
Intestinal Diseases
Intestinal Obstruction
Ileus
Intestinal Pseudo-Obstruction
Stomatognathic Diseases
Jaw Diseases
Mandibular Diseases
Craniomandibular Disorders
Temporomandibular Joint Disorders
Mouth Diseases
Facial Paralysis
Periodontal Diseases
Gingival Diseases
Gingivitis
Pharyngeal Diseases
Temporomandibular Joint Disorders
Tooth Diseases
Dental Deposits
Dental Plaque
Tooth Demineralization
Dental Caries
Respiratory Tract Diseases
Pleural Diseases
Pleural Effusion
Respiration Disorders
Respiratory Insufficiency
Otorhinolaryngologic Diseases
Pharyngeal Diseases
Deglutition Disorders
Nervous System Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Huntington Disease
Parkinsonian Disorders
Parkinson Disease
Brain Damage, Chronic
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Ataxias
Machado-Joseph Disease
Spinocerebellar Degenerations
Friedreich Ataxia
Spinocerebellar Ataxias
Machado-Joseph Disease
Dementia
Creutzfeldt-Jakob Syndrome
Huntington Disease
Epilepsy
Epilepsies, Myoclonic
Myoclonic Epilepsies, Progressive
Unverricht-Lundborg Syndrome
Central Nervous System Infections
Prion Diseases
Creutzfeldt-Jakob Syndrome
Movement Disorders
Dyskinesias
Chorea
Huntington Disease
Parkinsonian Disorders
Parkinson Disease
Spinal Cord Diseases
Amyotrophic Lateral Sclerosis
Muscular Atrophy, Spinal
Spinocerebellar Degenerations
Friedreich Ataxia
Spinocerebellar Ataxias
Machado-Joseph Disease
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Nystagmus, Congenital
Demyelinating Diseases
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Neurocutaneous Syndromes
Neurofibromatoses
Neurofibromatosis 1
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Huntington Disease
Myotonia Congenita
Myotonic Dystrophy
Neurofibromatoses
Neurofibromatosis 1
Spinocerebellar Degenerations
Friedreich Ataxia
Spinocerebellar Ataxias
Machado-Joseph Disease
Unverricht-Lundborg Syndrome
Motor Neuron Disease
Amyotrophic Lateral Sclerosis
Muscular Atrophy, Spinal
Parkinson Disease
Tauopathies
TDP-43 Proteinopathies
Amyotrophic Lateral Sclerosis
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Spinocerebellar Ataxias
Machado-Joseph Disease
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Intellectual Disability
Mental Retardation, X-Linked
Fragile X Syndrome
Neuromuscular Manifestations
Muscle Weakness
Muscular Atrophy
Myotonia
Paralysis
Facial Paralysis
Neuromuscular Diseases
Motor Neuron Disease
Amyotrophic Lateral Sclerosis
Muscular Atrophy, Spinal
Muscular Atrophy, Spinal
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Myotonic Disorders
Myotonia Congenita
Myotonic Dystrophy
Peripheral Nervous System Diseases
Neurofibromatosis 1
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Sleep Disorders
Dyssomnias
Sleep Disorders, Intrinsic
Disorders of Excessive Somnolence
Eye Diseases
Eye Abnormalities
Eyelid Diseases
Blepharoptosis
Lens Diseases
Cataract
Ocular Motility Disorders
Nystagmus, Pathologic
Nystagmus, Congenital
Male Urogenital Diseases
Genital Diseases, Male
Infertility
Infertility, Male
Oligospermia
Testicular Diseases
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Abortion, Spontaneous
Fetal Death
Fetal Diseases
Erythroblastosis, Fetal
Hydrops Fetalis
Polyhydramnios
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Marfan Syndrome
Heart Diseases
Arrhythmias, Cardiac
Atrial Flutter
Heart Block
Adams-Stokes Syndrome
Tachycardia
Tachycardia, Ventricular
Ventricular Fibrillation
Cardiomegaly
Cardiomyopathies
Heart Arrest
Death, Sudden, Cardiac
Heart Defects, Congenital
Marfan Syndrome
Heart Valve Diseases
Heart Valve Prolapse
Mitral Valve Prolapse
Mitral Valve Insufficiency
Myocardial Ischemia
Coronary Disease
Ventricular Dysfunction
Ventricular Dysfunction, Left
Vascular Diseases
Hypotension
Myocardial Ischemia
Coronary Disease
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Group Incompatibility
Erythroblastosis, Fetal
Hydrops Fetalis
Blood Protein Disorders
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Hydrops Fetalis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Marfan Syndrome
Waardenburg Syndrome
Cardiovascular Abnormalities
Heart Defects, Congenital
Marfan Syndrome
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Eye Abnormalities
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Foot Deformities, Congenital
Clubfoot
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Skin Abnormalities
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Fetal Diseases
Erythroblastosis, Fetal
Hydrops Fetalis
Genetic Diseases, Inborn
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Dwarfism
Achondroplasia
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Fragile X Syndrome
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Hydrops Fetalis
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Huntington Disease
Mental Retardation, X-Linked
Fragile X Syndrome
Myotonia Congenita
Myotonic Dystrophy
Neurofibromatoses
Neurofibromatosis 1
Spinocerebellar Degenerations
Friedreich Ataxia
Spinocerebellar Ataxias
Machado-Joseph Disease
Unverricht-Lundborg Syndrome
Marfan Syndrome
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Mannosidase Deficiency Diseases
alpha-Mannosidosis
Lysosomal Storage Diseases
Mannosidase Deficiency Diseases
alpha-Mannosidosis
Muscular Dystrophies
Myotonic Dystrophy
Neoplastic Syndromes, Hereditary
Neurofibromatoses
Neurofibromatosis 1
Skin Diseases, Genetic
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Infant, Newborn, Diseases
Infant, Premature, Diseases
Nystagmus, Congenital
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Marfan Syndrome
Skin Diseases
Skin Abnormalities
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Skin Diseases, Genetic
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Skin Diseases, Vesiculobullous
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Nutritional and Metabolic Diseases
Metabolic Diseases
Glucose Metabolism Disorders
Diabetes Mellitus
Hyperinsulinism
Insulin Resistance
Lipid Metabolism Disorders
Dyslipidemias
Hyperlipidemias
Hypercholesterolemia
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Mannosidase Deficiency Diseases
alpha-Mannosidosis
Lysosomal Storage Diseases
Mannosidase Deficiency Diseases
alpha-Mannosidosis
Mitochondrial Diseases
Friedreich Ataxia
Proteostasis Deficiencies
TDP-43 Proteinopathies
Amyotrophic Lateral Sclerosis
Endocrine System Diseases
Diabetes Mellitus
Gonadal Disorders
Testicular Diseases
Thyroid Diseases
Immune System Diseases
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Blood Group Incompatibility
Erythroblastosis, Fetal
Hydrops Fetalis
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Hypertrophy
Cardiomegaly
Pathologic Processes
Arrhythmias, Cardiac
Atrial Flutter
Heart Block
Adams-Stokes Syndrome
Tachycardia
Tachycardia, Ventricular
Ventricular Fibrillation
Chromosome Aberrations
Chromosomal Instability
Chromosome Fragility
Translocation, Genetic
Death
Death, Sudden
Death, Sudden, Cardiac
Fetal Death
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Anticipation, Genetic
Diseases in Twins
Facies
Recurrence
Genomic Instability
Chromosomal Instability
Chromosome Fragility
Hemorrhage
Hematoma
Muscle Weakness
Signs and Symptoms
Edema
Hydrops Fetalis
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Intellectual Disability
Neuromuscular Manifestations
Muscle Weakness
Muscular Atrophy
Myotonia
Paralysis
Facial Paralysis
Signs and Symptoms, Respiratory
Anoxia
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