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familial hemolytic anemia

Go to external page http://purl.obolibrary.org/obo/MONDO_0003689

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

Synonyms: congenital hemolytic anaemia hereditary hemolytic anaemia hereditary hemolytic anemia congenital hemolytic anemia

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:282 (DOID:589)
  • ICD9:282.9 (DOID:589)
  • MEDGEN:1919 (MONDO:equivalentTo)
  • GARD:6167 (MONDO:GARD)
  • UMLS:C0002881 (MONDO:equivalentTo)
  • MESH:D000745 (MONDO:equivalentTo)
  • NANDO:2100183 (https://orcid.org/0000-0003-0011-764X)
  • DOID:589 (MONDO:equivalentTo)
  • NCIT:C34379 (MONDO:equivalentTo)
  • SCTID:42601008 (MONDO:equivalentTo)
Subsets

gard_rare, otar, rare

exactMatch

http://identifiers.org/snomedct/42601008

http://purl.obolibrary.org/obo/NCIT_C34379

http://identifiers.org/medgen/1919

http://purl.obolibrary.org/obo/DOID_589

http://linkedlifedata.com/resource/umls/id/C0002881

http://identifiers.org/mesh/D000745

has related synonym

anaemia hemolytic congenital

anemia hemolytic congenital

id

MONDO:0003689

seeAlso

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

Term relations