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Query OMIM entry list
141750
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ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, DELETION-TYPE
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Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Digestive System Diseases
Liver Diseases
Hepatomegaly
Nervous System Diseases
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Male Urogenital Diseases
Genital Diseases, Male
Penile Diseases
Hypospadias
Urogenital Abnormalities
Hypospadias
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urogenital Abnormalities
Hypospadias
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Ductus Arteriosus, Patent
Heart Diseases
Heart Defects, Congenital
Ductus Arteriosus, Patent
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Thalassemia
alpha-Thalassemia
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Cardiovascular Abnormalities
Heart Defects, Congenital
Ductus Arteriosus, Patent
Chromosome Disorders
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Urogenital Abnormalities
Hypospadias
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Thalassemia
alpha-Thalassemia
Chromosome Disorders
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Hepatomegaly
Splenomegaly
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Translocation, Genetic
Disease
Syndrome
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
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