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310200
DMD
MUSCULAR DYSTROPHY, DUCHENNE TYPE
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Marfan Syndrome
Joint Diseases
Contracture
Hip Contracture
Muscular Diseases
Contracture
Hip Contracture
Muscle Cramp
Muscle Weakness
Muscular Disorders, Atrophic
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Rhabdomyolysis
Myoglobinuria
Digestive System Diseases
Gastrointestinal Diseases
Intestinal Diseases
Intestinal Obstruction
Stomach Diseases
Gastric Dilatation
Nervous System Diseases
Central Nervous System Diseases
Movement Disorders
Spinal Cord Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Psychomotor Disorders
Neuromuscular Manifestations
Muscle Cramp
Muscle Weakness
Sensation Disorders
Vision Disorders
Color Vision Defects
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Peripheral Nervous System Diseases
Eye Diseases
Eye Diseases, Hereditary
Albinism
Albinism, Ocular
Retinitis Pigmentosa
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Vision Disorders
Color Vision Defects
Night Blindness
Male Urogenital Diseases
Urogenital Abnormalities
Disorders of Sex Development
Gonadal Dysgenesis
Turner Syndrome
Sex Chromosome Disorders of Sex Development
Klinefelter Syndrome
Turner Syndrome
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urogenital Abnormalities
Disorders of Sex Development
Gonadal Dysgenesis
Turner Syndrome
Sex Chromosome Disorders of Sex Development
Klinefelter Syndrome
Turner Syndrome
Pregnancy Complications
Fetal Diseases
Obstetric Labor Complications
Breech Presentation
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Marfan Syndrome
Turner Syndrome
Heart Diseases
Arrhythmias, Cardiac
Cardiomegaly
Cardiomyopathy, Dilated
Cardiomyopathies
Cardiomyopathy, Dilated
Heart Defects, Congenital
Marfan Syndrome
Turner Syndrome
Heart Valve Diseases
Heart Valve Prolapse
Mitral Valve Prolapse
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Hemophilia A
Coagulation Protein Disorders
Hemophilia A
Hemorrhagic Disorders
Hemophilia A
Leukocyte Disorders
Phagocyte Bactericidal Dysfunction
Granulomatous Disease, Chronic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Marfan Syndrome
Cardiovascular Abnormalities
Heart Defects, Congenital
Marfan Syndrome
Turner Syndrome
Chromosome Disorders
Sex Chromosome Disorders
Sex Chromosome Disorders of Sex Development
Klinefelter Syndrome
Turner Syndrome
Skin Abnormalities
Ichthyosis
Urogenital Abnormalities
Disorders of Sex Development
Gonadal Dysgenesis
Turner Syndrome
Sex Chromosome Disorders of Sex Development
Klinefelter Syndrome
Turner Syndrome
Fetal Diseases
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Hemophilia A
Chromosome Disorders
Sex Chromosome Disorders
Sex Chromosome Disorders of Sex Development
Klinefelter Syndrome
Turner Syndrome
Eye Diseases, Hereditary
Albinism
Albinism, Ocular
Retinitis Pigmentosa
Genetic Diseases, X-Linked
Granulomatous Disease, Chronic
Mental Retardation, X-Linked
Muscular Dystrophy, Duchenne
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Marfan Syndrome
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Ocular
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Skin Diseases, Genetic
Albinism
Albinism, Ocular
Infant, Newborn, Diseases
Ichthyosis
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Marfan Syndrome
Skin Diseases
Keratosis
Ichthyosis
Pigmentation Disorders
Hypopigmentation
Albinism
Albinism, Ocular
Skin Abnormalities
Ichthyosis
Skin Diseases, Genetic
Albinism
Albinism, Ocular
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Ocular
Water-Electrolyte Imbalance
Hypokalemia
Endocrine System Diseases
Adrenal Gland Diseases
Adrenal Insufficiency
Gonadal Disorders
Disorders of Sex Development
Gonadal Dysgenesis
Turner Syndrome
Sex Chromosome Disorders of Sex Development
Klinefelter Syndrome
Turner Syndrome
Hypogonadism
Klinefelter Syndrome
Immune System Diseases
Immunologic Deficiency Syndromes
Phagocyte Bactericidal Dysfunction
Granulomatous Disease, Chronic
Animal Diseases
Disease Models, Animal
Muscular Dystrophy, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Arrhythmias, Cardiac
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosome Breakage
Chromosome Inversion
Sex Chromosome Aberrations
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Acute Disease
Disease Susceptibility
Genetic Predisposition to Disease
Diseases in Twins
Fibrosis
Growth Disorders
Inflammation
Ischemia
Muscle Weakness
Necrosis
Signs and Symptoms
Body Weight
Birth Weight
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Neuromuscular Manifestations
Muscle Cramp
Muscle Weakness
Sensation Disorders
Vision Disorders
Color Vision Defects
Signs and Symptoms, Digestive
Vomiting
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