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306700
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HEMOPHILIA A
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Virus Diseases
DNA Virus Infections
Hepadnaviridae Infections
Hepatitis B
Hepatitis, Viral, Human
Hepatitis B
Neoplasms
Neoplasms by Histologic Type
Leukemia
Leukemia, Lymphoid
Leukemia, T-Cell
Neoplasms by Site
Thoracic Neoplasms
Respiratory Tract Neoplasms
Lung Neoplasms
Musculoskeletal Diseases
Joint Diseases
Arthritis
Arthritis, Rheumatoid
Hemarthrosis
Synovitis
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Rheumatic Diseases
Arthritis, Rheumatoid
Digestive System Diseases
Liver Diseases
Hepatitis
Hepatitis, Viral, Human
Hepatitis B
Respiratory Tract Diseases
Lung Diseases
Lung Neoplasms
Respiratory Tract Neoplasms
Lung Neoplasms
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lesch-Nyhan Syndrome
Cerebrovascular Disorders
Intracranial Hemorrhages
Cerebral Hemorrhage
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Lesch-Nyhan Syndrome
Neurologic Manifestations
Neurobehavioral Manifestations
Memory Disorders
Intellectual Disability
Mental Retardation, X-Linked
Fragile X Syndrome
Lesch-Nyhan Syndrome
Sensation Disorders
Vision Disorders
Color Vision Defects
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Eye Diseases
Vision Disorders
Color Vision Defects
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Diabetes Insipidus
Urination Disorders
Enuresis
Urinary Incontinence
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Diabetes Insipidus
Urination Disorders
Enuresis
Urinary Incontinence
Pregnancy Complications
Fetal Diseases
Cardiovascular Diseases
Heart Diseases
Myocardial Ischemia
Coronary Disease
Myocardial Infarction
Vascular Diseases
Cerebrovascular Disorders
Intracranial Hemorrhages
Cerebral Hemorrhage
Myocardial Ischemia
Coronary Disease
Myocardial Infarction
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Anemia, Sickle Cell
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Afibrinogenemia
Factor XIII Deficiency
Hemophilia A
Hemophilia B
von Willebrand Diseases
Coagulation Protein Disorders
Afibrinogenemia
Factor XIII Deficiency
Hemophilia A
Hemophilia B
von Willebrand Diseases
Blood Platelet Disorders
von Willebrand Diseases
Hemoglobinopathies
Anemia, Sickle Cell
Hemorrhagic Disorders
Afibrinogenemia
Factor XIII Deficiency
Hemophilia A
Hemophilia B
von Willebrand Diseases
Lymphatic Diseases
Lymphoproliferative Disorders
Leukemia, Lymphoid
Leukemia, T-Cell
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Incontinentia Pigmenti
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Skin Abnormalities
Incontinentia Pigmenti
Fetal Diseases
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Anemia, Sickle Cell
Blood Coagulation Disorders, Inherited
Afibrinogenemia
Factor XIII Deficiency
Hemophilia A
Hemophilia B
von Willebrand Diseases
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Genetic Diseases, X-Linked
Hemophilia B
Mental Retardation, X-Linked
Fragile X Syndrome
Lesch-Nyhan Syndrome
Hemoglobinopathies
Anemia, Sickle Cell
Heredodegenerative Disorders, Nervous System
Lesch-Nyhan Syndrome
Mental Retardation, X-Linked
Fragile X Syndrome
Lesch-Nyhan Syndrome
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Lesch-Nyhan Syndrome
Purine-Pyrimidine Metabolism, Inborn Errors
Lesch-Nyhan Syndrome
Muscular Dystrophies
Skin Diseases, Genetic
Incontinentia Pigmenti
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Rheumatic Diseases
Arthritis, Rheumatoid
Skin Diseases
Pigmentation Disorders
Incontinentia Pigmenti
Skin Abnormalities
Incontinentia Pigmenti
Skin Diseases, Genetic
Incontinentia Pigmenti
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lesch-Nyhan Syndrome
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Lesch-Nyhan Syndrome
Purine-Pyrimidine Metabolism, Inborn Errors
Lesch-Nyhan Syndrome
Endocrine System Diseases
Pituitary Diseases
Diabetes Insipidus
Immune System Diseases
Autoimmune Diseases
Arthritis, Rheumatoid
Immunoproliferative Disorders
Lymphoproliferative Disorders
Leukemia, Lymphoid
Leukemia, T-Cell
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosome Inversion
Sex Chromosome Aberrations
Translocation, Genetic
Disease
Disease Attributes
Chronic Disease
Disease Susceptibility
Genetic Predisposition to Disease
Hemorrhage
Blood Loss, Surgical
Hemarthrosis
Intracranial Hemorrhages
Cerebral Hemorrhage
Intraoperative Complications
Blood Loss, Surgical
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Memory Disorders
Sensation Disorders
Vision Disorders
Color Vision Defects
Urological Manifestations
Lower Urinary Tract Symptoms
Urinary Incontinence
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