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110700
FY
BLOOD GROUP--DUFFY SYSTEM
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Bacterial Infections and Mycoses
Infection
Communicable Diseases
Virus Diseases
RNA Virus Infections
Retroviridae Infections
Lentivirus Infections
HIV Infections
Sexually Transmitted Diseases
Sexually Transmitted Diseases, Viral
HIV Infections
Parasitic Diseases
Protozoan Infections
Malaria
Malaria, Falciparum
Malaria, Vivax
Neoplasms
Neoplasms by Site
Breast Neoplasms
Thoracic Neoplasms
Respiratory Tract Neoplasms
Lung Neoplasms
Urogenital Neoplasms
Genital Neoplasms, Male
Prostatic Neoplasms
Neoplastic Processes
Neoplasm Metastasis
Respiratory Tract Diseases
Lung Diseases
Lung Neoplasms
Respiratory Tract Neoplasms
Lung Neoplasms
Nervous System Diseases
Central Nervous System Diseases
Spinal Cord Diseases
Muscular Atrophy, Spinal
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Motor Neuron Disease
Muscular Atrophy, Spinal
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Muscular Atrophy, Spinal
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Male Urogenital Diseases
Genital Diseases, Male
Genital Neoplasms, Male
Prostatic Neoplasms
Prostatic Diseases
Prostatic Neoplasms
Urogenital Neoplasms
Genital Neoplasms, Male
Prostatic Neoplasms
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Diseases
Erythroblastosis, Fetal
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Anemia, Sickle Cell
Sickle Cell Trait
Thalassemia
alpha-Thalassemia
Blood Group Incompatibility
Erythroblastosis, Fetal
Hemoglobinopathies
Anemia, Sickle Cell
Sickle Cell Trait
Thalassemia
alpha-Thalassemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Fetal Diseases
Erythroblastosis, Fetal
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Anemia, Sickle Cell
Sickle Cell Trait
Thalassemia
alpha-Thalassemia
Chromosome Disorders
Hemoglobinopathies
Anemia, Sickle Cell
Sickle Cell Trait
Thalassemia
alpha-Thalassemia
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Lysosomal Storage Diseases
Mucopolysaccharidoses
Infant, Newborn, Diseases
Erythroblastosis, Fetal
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Mucinoses
Mucopolysaccharidoses
Skin Diseases
Breast Diseases
Breast Neoplasms
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Lysosomal Storage Diseases
Mucopolysaccharidoses
Immune System Diseases
Blood Group Incompatibility
Erythroblastosis, Fetal
Immunologic Deficiency Syndromes
HIV Infections
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Trisomy
Chromosomal Instability
Chromosome Fragility
Chromosome Duplication
Trisomy
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Genomic Instability
Chromosomal Instability
Chromosome Fragility
Neoplastic Processes
Neoplasm Metastasis
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
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