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Ontology Browser

Term:
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to (DOID:9004820)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
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  

Synonyms
Exact Synonyms: Hemolytic Anemia due to P5N Deficiency ;   Hemolytic Anemia due to UMPH1 Deficiency ;   P5N DEFICIENCY ;   Pyrimidine 5-Prime Nucleotidase Deficiency, Hemolytic Anemia due to ;   UMPH1 Deficiency
Primary IDs: MESH:C564859 ;   RDO:0013679
Alternate IDs: OMIM:266120

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