MeSH Treeview
Query OMIM entry list
601814
FXYD2
FXYD DOMAIN-CONTAINING ION TRANSPORT REGULATOR 2
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High-scoring List
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glycogen Storage Disease
Glycogen Storage Disease Type I
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glycogen Storage Disease
Glycogen Storage Disease Type I
Nutrition Disorders
Malnutrition
Deficiency Diseases
Magnesium Deficiency
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Database Center for Life Science
