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Ontology Browser

Term:
Rh-Null Disease, Amorph Type (DOID:9003229)
Annotations: Rat: (0) Mouse: (0) Human: (1) Chinchilla: (1) Bonobo: (0) 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  
The amorph RH-null phenotype arises from mutations at the RH locus itself that silence Rh expression and cause mild to moderate hemolytic anemia. Red blood cells exhibit characteristic morphologic and functional abnormalities including spherocytosis, stomatocytosis, and diminished lifespan. (OMIM)
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: RH-null, amorph type ;   RHNA ;   amorph type of RH-null phenotype
Related Synonyms: BLOOD GROUP--RHESUS SYSTEM Cc/Ee POLYPEPTIDE ;   RHESUS BLOOD GROUP, CcEe ANTIGENS
Primary IDs: MESH:C566210
Alternate IDs: OMIM:111700 ;   OMIM:617970

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