| Disease Browser
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Parent Node:
 Intestinal Diseases (D007410) |
Parent Node:
Metabolic Diseases (D008659) |
..Starting node
.. Malabsorption Syndromes (D008286)
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Child Nodes:
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| ........Blind Loop Syndrome (D001765) |
| ........Celiac Disease (D002446) |
| ........Chylomicron retention disease (C535460) |
| ........Collagenous Sprue (D064068) |
| ........Diarrhea 4, Malabsorptive, Congenital (C563673) |
| ........Diarrhea 5, With Tufting Enteropathy, Congenital (C567703) |
| ........Folate Malabsorption, Hereditary (C562799) |
| ........Glucose-Galactose Malabsorption (C562602) |
........Hyperhomocysteinemia (D020138)  8 |
| ........Imerslund-Grasbeck syndrome (C538556) 1 |
| ........Lactose Intolerance (D007787) 1 |
| ........Lysine Malabsorption Syndrome (C563080) |
| ........Microvillus inclusion disease (C537470) |
| ........Short Bowel Syndrome (D012778) |
| ........Sprue, Tropical (D013182) |
| ........Steatorrhea (D045602) 1 |
| ........Whipple Disease (D008061) 1 |
Sister Nodes: |
..Acid-Base Imbalance (D000137) 42
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..ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 2 (OMIM:606770)
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..ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 3 (OMIM:606771)
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..Brain Diseases, Metabolic (D001928) 244
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..Calcium Metabolism Disorders (D002128) 94
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..DNA Repair-Deficiency Disorders (D049914) 95
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..Glucose Metabolism Disorders (D044882) 137
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..Hyperlactatemia (D065906)
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..Hypermanganesemia with Dystonia Polycythemia and Cirrhosis (C548016)
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..Iron Metabolism Disorders (D019189) 23
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..Lipid Metabolism Disorders (D052439) 189
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..Malabsorption Syndromes (D008286) 29
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..Metabolic Syndrome X (D024821) 1
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..Metabolism, Inborn Errors (D008661) 886
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..Mitochondrial Diseases (D028361) 114
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..Phosphorus Metabolism Disorders (D010760) 25
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..Porphyrias (D011164) 18
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..Proteostasis Deficiencies (D057165) 55
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..SHORT syndrome (C537327)
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..Skin Diseases, Metabolic (D012875) 33
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..Wasting Syndrome (D019282) 1
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..Water-Electrolyte Imbalance (D014883) 31
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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