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congenital nonspherocytic hemolytic anemia

Go to external page http://purl.obolibrary.org/obo/MONDO_0006506

Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. Common causes include deficiencies in glucose-6-phosphate isomerase; pyruvate kinase; and glucose-6-phosphate dehydrogenase. [ MESH:D000746 ]

Synonyms: hereditary nonspherocytic hemolytic anemia hereditary nonspherocytic hemolytic anaemia HNSHA

This is just here as a test because I lose it

Term information

database cross reference
  • DOID:2861 (MONDO:equivalentTo)
  • ICD9:282.3 (MONDO:relatedTo)
  • MESH:D000746 (MONDO:equivalentTo)
  • UMLS:C0002882 (MONDO:equivalentTo)
  • SCTID:301317008 (MONDO:equivalentTo)
  • EFO:1000641 (MONDO:equivalentTo)
  • MEDGEN:284 (MONDO:equivalentTo)
Subsets

gard_rare, otar, rare

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/4069

exactMatch

http://purl.obolibrary.org/obo/DOID_2861

http://identifiers.org/mesh/D000746

http://identifiers.org/snomedct/301317008

http://identifiers.org/medgen/284

http://linkedlifedata.com/resource/umls/id/C0002882

id

MONDO:0006506