FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hereditary elliptocytosis ID (Ontology) DOID:2373 (Human Disease)
Definition A hematopoietic system disease characterized by oval or elliptical red blood cells, slight or absent hemolysis with little or no anemia; splenomegaly is often present.
Also Known As "Congenital elliptocytosis" ; "ovalocytosis"
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 Genes
 hereditary elliptocytosis       2
 for disease ribbon | hereditary elliptocytosis       2
 model of | hereditary elliptocytosis       2
Spanning Tree (Parents/Children)
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  disease of anatomical entity
   |__hematopoietic system disease
       |__hereditary elliptocytosis  2 rec.
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Is a hematopoietic system disease
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Synonyms
  • "Congenital elliptocytosis" EXACT
    "ovalocytosis" EXACT
Secondary IDs
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GARD:6621
ICD10CM:D58.1
ICD9CM:282.1
MESH:D004612
MIM:130600
MIM:611804
NCI:C35882
ORDO:288
SNOMEDCT_US_2023_03_01:154801000
UMLS_CUI:C0013902