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314700
XG
XG BLOOD GROUP SYSTEM
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Osteochondrodysplasias
Chondrodysplasia Punctata
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Nervous System Diseases
Neurologic Manifestations
Sensation Disorders
Vision Disorders
Color Vision Defects
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Eye Diseases
Vision Disorders
Color Vision Defects
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Glucosephosphate Dehydrogenase Deficiency
Anemia, Hypochromic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Skin Abnormalities
Ichthyosis
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Glucosephosphate Dehydrogenase Deficiency
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Muscular Dystrophies
Infant, Newborn, Diseases
Ichthyosis
Skin and Connective Tissue Diseases
Skin Diseases
Keratosis
Ichthyosis
Skin Abnormalities
Ichthyosis
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Sex Chromosome Aberrations
Translocation, Genetic
Signs and Symptoms
Neurologic Manifestations
Sensation Disorders
Vision Disorders
Color Vision Defects
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