Search Ontology:

Human Disease

congenital hemolytic anemia

Term ID

DOID:589

Synonyms

congenital hemolytic anaemia
hereditary hemolytic anaemia
hereditary hemolytic anemia

Definition

References

GARD:6167
ICD10CM:D58.9
ICD9CM:282
MESH:D000745
NCI:C34379
SNOMEDCT_US_2023_03_01:42601008
UMLS_CUI:C0002881

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Ontology

Human Disease ( DOID:589 )

Relationships

is a type of: hemolytic anemia physical disorder

hemolytic anemia physical disorder Show first 5 Terms
has subtype: congenital dyserythropoietic anemia congenital nonspherocytic hemolytic anemia hemoglobinopathy hereditary spherocytosis X-linked congenital hemolytic anemia

congenital dyserythropoietic anemia congenital nonspherocytic hemolytic anemia hemoglobinopathy hereditary spherocytosis X-linked congenital hemolytic anemia Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models