MeSH Treeview
Query OMIM entry list
301300
-
ANEMIA, SIDEROBLASTIC, X-LINKED
→
High-scoring List
Neoplasms
Neoplasms by Histologic Type
Leukemia
Leukemia, Myeloid
Leukemia, Myeloid, Acute
Leukemia, Erythroblastic, Acute
Nervous System Diseases
Neurologic Manifestations
Dyskinesias
Ataxia
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Renal Insufficiency
Renal Insufficiency, Chronic
Kidney Failure, Chronic
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Renal Insufficiency
Renal Insufficiency, Chronic
Kidney Failure, Chronic
Cardiovascular Diseases
Vascular Diseases
Arterial Occlusive Diseases
Arteriosclerosis
Hypertension
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Glucosephosphate Dehydrogenase Deficiency
Thalassemia
Anemia, Hypochromic
Anemia, Macrocytic
Anemia, Refractory
Anemia, Sideroblastic
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Wiskott-Aldrich Syndrome
Bone Marrow Diseases
Myelodysplastic Syndromes
Anemia, Refractory
Anemia, Sideroblastic
Myeloproliferative Disorders
Leukemia, Erythroblastic, Acute
Hemoglobinopathies
Thalassemia
Hemorrhagic Disorders
Wiskott-Aldrich Syndrome
Leukocyte Disorders
Leukopenia
Lymphopenia
Wiskott-Aldrich Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Glucosephosphate Dehydrogenase Deficiency
Thalassemia
Blood Coagulation Disorders, Inherited
Wiskott-Aldrich Syndrome
Genetic Diseases, X-Linked
Wiskott-Aldrich Syndrome
Hemoglobinopathies
Thalassemia
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Lipid Metabolism, Inborn Errors
Hypolipoproteinemias
Metal Metabolism, Inborn Errors
Hemochromatosis
Progeria
Nutritional and Metabolic Diseases
Metabolic Diseases
Glucose Metabolism Disorders
Diabetes Mellitus
Diabetes Mellitus, Type 2
Diabetes Mellitus, Lipoatrophic
Hyperinsulinism
Insulin Resistance
Iron Metabolism Disorders
Iron Overload
Hemochromatosis
Hemosiderosis
Lipid Metabolism Disorders
Dyslipidemias
Hyperlipidemias
Hypolipoproteinemias
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Lipid Metabolism, Inborn Errors
Hypolipoproteinemias
Metal Metabolism, Inborn Errors
Hemochromatosis
Progeria
Nutrition Disorders
Malnutrition
Deficiency Diseases
Avitaminosis
Vitamin B Deficiency
Vitamin B 6 Deficiency
Endocrine System Diseases
Diabetes Mellitus
Diabetes Mellitus, Type 2
Diabetes Mellitus, Lipoatrophic
Immune System Diseases
Graft vs Host Disease
Immunologic Deficiency Syndromes
Lymphopenia
Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Translocation, Genetic
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Hyperplasia
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Database Center for Life Science
