Ontology Browser

mineral metabolism disease (DOID:0050032)
Annotations: Rat: (410) Mouse: (411) Human: (452) Chinchilla: (376) Bonobo: (400) Dog: (398) Squirrel: (383)
Parent Terms Term With Siblings Child Terms
Acid-Base Imbalance +   
acquired metabolic disease +   
amyloidosis +   
carbohydrate metabolism disease +   
DNA Repair-Deficiency Disorders +   
glucose metabolism disease +   
Hypermanganesemia with Dystonia, Polycythemia and Cirrhosis +   
hyperprolactinemia +   
hyperuricemia +   
inherited metabolic disorder +   
lipid metabolism disorder +   
Malabsorption Syndromes +   
metabolic acidosis +   
Metabolic Bone Diseases +   
Metabolic Brain Diseases +   
Metabolic Skin Diseases +   
Metabolic Syndrome +   
mineral metabolism disease +   
An acquired metabolic disease that is characterized by abnormal mineral metabolism. (DO)
mitochondrial metabolism disease +   
nutrition disease +   
phosphorus metabolism disease +   
porphyria +   
Proteostasis Deficiencies +   
Reperfusion Injury +   
SHORT Syndrome  
Wasting Syndrome +   
Water-Electrolyte Imbalance +   

Primary IDs: RDO:9003951
Definition Sources: http://www.nlm.nih.gov/medlineplus/metabolicdisorders.html

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.