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DO Term : hereditary elliptocytosis [DOID:2373] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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.

synonyms:
UMLS_CUI:C0013902,
ICD9CM:282.1,
MESH:D004612,
SNOMEDCT_US_2023_03_01:154801000,
ICD10CM:D58.1,
GARD:6621,
ORDO:288,
Congenital elliptocytosis,
ovalocytosis,
130600,
OMIM:130600,
611804,
OMIM:611804,
NCI:C35882

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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