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pure red-cell aplasia

Go to external page http://purl.obolibrary.org/obo/MONDO_0001705

A disease characterized by normocytic, normochromic anemia, low hematocrit, reticulocytopenia, and selective erythroid hypoplasia. [ NCIT:P378 ]

Synonyms: primary red cell aplasia red cell hypoplasia PRCA pure red cell aplasia

This is just here as a test because I lose it

Term information

database cross reference
  • MESH:D012010 (MONDO:equivalentTo)
  • SCTID:50715003 (MONDO:equivalentTo)
  • NCIT:C34974 (MONDO:equivalentTo)
  • DOID:1340 (MONDO:equivalentTo)
  • NORD:1636 (MONDO:NORD)
  • ICD9:284.81 (MONDO:relatedTo)
  • UMLS:C0034902 (NCIT:C34974)
Subsets

rare, nord_rare

exactMatch

http://identifiers.org/snomedct/50715003

http://identifiers.org/mesh/D012010

http://linkedlifedata.com/resource/umls/id/C0034902

http://purl.obolibrary.org/obo/NCIT_C34974

http://purl.obolibrary.org/obo/DOID_1340

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0012197

id

MONDO:0001705

Term relations

Subclass of: