OBO ID: DOID:2373
Term Name: hereditary elliptocytosis Search Ontology:
Synonyms:
  • Congenital elliptocytosis
  • ovalocytosis
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. (3)
References:
Ontology: Human Disease   ( DOID:2373 )
Relationships
is a type of:
OTHER hereditary elliptocytosis PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
EPB41 Elliptocytosis-1 611804
SPTA1 Elliptocytosis-2
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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