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Ontology Browser

Term:
Red Cell Phospholipid Defect with Hemolysis (DOID:9006910)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
Hemolysis +     
congenital dyserythropoietic anemia +   
Congenital Hemolytic Anemia with Emphysema and Cutis Laxa 
congenital nonspherocytic hemolytic anemia +   
dehydrated hereditary stomatocytosis +   
glucosephosphate dehydrogenase deficiency +   
hemoglobinopathy +   
hereditary elliptocytosis +   
hereditary spherocytosis +   
Nonspherocytic Hemolytic Anemia due to Glucose Phosphate Isomerase Deficiency  
overhydrated hereditary stomatocytosis  
Red Cell Phospholipid Defect with Hemolysis 
Rh-Null Disease, Amorph Type  
sickle cell anemia +   
Stomatocytosis II  
thalassemia +   
Transient Erythroblastopenia of Childhood 
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to  
X-linked congenital hemolytic anemia  
X-linked thrombocytopenia with beta-thalassemia  

Synonyms
Exact Synonyms: High red cell phosphatidylcholine hemolytic anemia ;   Leaky Red cell syndrome ;   Phosphatidylcholine Red cell membrane disorder
Primary IDs: MESH:C535298 ;   RDO:0000331

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