Search Ontology:
Human Disease

pure red-cell aplasia

Term ID
DOID:1340
Synonyms
  • primary red cell aplasia
  • pure red cell aplasia
  • Red cell hypoplasia
Definition
A congenital hypoplastic anemia that is characterized by a normocytic normochromic anemia with severe reticulocytopenia and marked reduction or absence of erythroid precursors from the bone marrow. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6142432/
References
  • GARD:7504
  • MESH:D012010
  • NCI:C34974
  • SNOMEDCT_US_2023_03_01:191252000
  • UMLS_CUI:C0034902
Ontology
Human Disease   ( DOID:1340 )
Relationships
is a type of
has subtype
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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