MeSH Treeview
Query OMIM entry list
145981
HHC2
HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors
Nutritional and Metabolic Diseases
Metabolic Diseases
Calcium Metabolism Disorders
Hypercalcemia
Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors
Water-Electrolyte Imbalance
Hypercalcemia
Endocrine System Diseases
Parathyroid Diseases
Hyperparathyroidism
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