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familial hemolytic anemia

^ http://purl.obolibrary.org/obo/MONDO_0003689

A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies. [ NCIT:C34379 ]

Term info

database cross reference
  • NCIT:C34379 (MONDO:equivalentTo)
  • MESH:D000745 (MONDO:equivalentTo)
  • SCTID:42601008 (MONDO:equivalentTo)
  • ICD9:282.9 (DOID:589)
  • GARD:0006167 (MONDO:equivalentTo)
  • DOID:589 (MONDO:equivalentTo)
  • ICD9:282 (DOID:589)
Subsets

gard_rare

definition

A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies.

exactMatch

http://identifiers.org/snomedct/42601008, http://purl.obolibrary.org/obo/NCIT_C34379, http://purl.obolibrary.org/obo/DOID_589, http://identifiers.org/mesh/D000745

has exact synonym

hereditary hemolytic anemia, congenital hemolytic anemia

has related synonym

anemia hemolytic congenital

id

MONDO:0003689

seeAlso

https://rarediseases.info.nih.gov/diseases/6167/congenital-hemolytic-anemia

Term relations