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Ontology Browser

Parent Terms Term With Siblings Child Terms
acquired night blindness 
Avitaminosis +   
biotin deficiency 
Combined Immunodeficiency and Megaloblastic Anemia with or without Hyperhomocysteinemia  
congenital intrinsic factor deficiency  
copper deficiency myelopathy 
Cystic Fibrosis with Helicobacter Pylori Gastritis, Megaloblastic Anemia, and Subnormal Mentality 
endemic goiter 
Folate-Responsive Megaloblastic Anemia  
folic acid deficiency anemia +   
homocystinuria-megaloblastic anemia cblE type  
Imerslund-Grasbeck Syndrome +   
iron deficiency anemia +   
Keshan disease  
Lubani Al Saleh Teebi Syndrome 
Megaloblastic Anemia due to Dihydrofolate Reductase Deficiency  
methylmalonic aciduria and homocystinuria type cblC  
pernicious anemia +   
A megaloblastic anemia occurring in children but more commonly in later life, characterized by histamine-fast achlorhydria, in which the laboratory and clinical manifestations are based on malabsorption of vitamin B 12 due to a failure of the gastric mucosa to secrete adequate and potent intrinsic factor. (Dorland, 27th ed)
Potassium Deficiency  
primary hypomagnesemia +   
Protein Deficiency +   
protein-energy malnutrition +   
pyridoxine deficiency anemia  
riboflavin deficiency  
Subacute Combined Degeneration  
thiamine-responsive megaloblastic anemia syndrome  
transcobalamin II deficiency  
Zinc Deficiency +   

Exact Synonyms: Addison anemia ;   Addison's anaemia ;   Addison's anemia ;   Addisons anemia ;   Biermer's anaemia ;   Biermer's anemia ;   pernicious anaemia
Primary IDs: MESH:D000752
Alternate IDs: OMIM:170900
Xrefs: GARD:12671 ;   ICD10CM:D51.0 ;   ICD9CM:281.0 ;   NCI:C2871
Definition Sources: "DO" "DO", "DO" "DO", MESH:D000752

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