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Ontology Browser

hereditary spherocytosis (DOID:12971)
Annotations: Rat: (11) Mouse: (11) Human: (11) Chinchilla: (9) Bonobo: (10) Dog: (10) Squirrel: (10) Pig: (10)
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 +   
Familial Obstructive Jaundice of Infancy 
glucosephosphate dehydrogenase deficiency +   
hemoglobinopathy +   
hereditary elliptocytosis +   
hereditary spherocytosis +   
A group of familial congenital hemolytic anemias characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions.
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  

Exact Synonyms: Debrie's familial haemolytic disease ;   HS ;   Hereditary Spherocytic Hemolytic Anemia ;   Minkowski Chauffard syndrome ;   Minkowski-Chauffard disease ;   Minkowski-Chauffard haemolytic jaundice ;   Minkowski-Chauffard-Gänsslen syndrome ;   acholuric jaundice ;   chronic acholuric jaundice ;   congenital hemolytic jaundice ;   congenital spherocytic hemolytic anemia ;   congenital spherocytosis ;   hereditary spherocytoses ;   spherocytic anemia
Narrow Synonyms: spherocytosis, dominant ;   spherocytosis, recessive
Primary IDs: MESH:D013103
Alternate IDs: MESH:C536356
Xrefs: GARD:6639 ;   ICD10CM:D58.0 ;   ICD9CM:282.0 ;   NCI:C97074 ;   ORDO:822
Definition Sources: "DO", MESH:D013103

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