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Leukoerythroblastic Anemia (CUI C0002890) Suggest changes to this concept
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Terms & Properties

Concept Unique Identifier (CUI): C0002890

NCI Thesaurus Code: C36218  (see NCI Thesaurus info)

Semantic Type: Disease or Syndrome

NCIt Definition: A laboratory test result indicating the presence of nucleated red blood cells and immature leukocytes in the peripheral blood. It is observed in disorders causing extramedullary hematopoiesis such as myelofibrosis and metastatic cancer to the bone marrow.

MSH Definition: Anemia characterized by appearance of immature myeloid and nucleated erythrocytes in the peripheral blood, resulting from infiltration of the bone marrow by foreign or abnormal tissue.

Synonyms & Abbreviations: (see Synonym Details)
Anaemia associated with marrow infiltration
Anaemia leukoerythroblastic
Anemia associated with marrow infiltration
ANEMIA LEUKOERYTHROBLASTIC
ANEMIA, LEUKOERYTHROBLASTIC
ANEMIA, MYELOPATHIC
Anemia, Myelophthisic [Disease/Finding]
ANEMIA, MYELOPHTHISIC
Anemias, Leukoerythroblastic
Anemias, Myelophthisic
Leucoerythroblastic anaemia
Leucoerythroblastic anemia
Leukoerythroblastic anaemia
Leukoerythroblastic Anemias
Leukoerythroblastic anemia
Leukoerythroblastic Reaction
LEUKOERYTHROBLASTOSIS
Myelophthisic anaemia
Myelophthisic anemia (disorder)
Myelophthisic Anemias
Myelophthisic anemia

External Source Codes: 
NCI Thesaurus Code C36218 (see NCI Thesaurus info)

Other Properties: Property Definitions
Name Value Source
ACTIVE 1 SNOMEDCT_US
AQL BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI MSH
CASE_SIGNIFICANCE_ID 900000000000448009 SNOMEDCT_US
CTV3ID D21y2 SNOMEDCT_US
DC 1 MSH
DEFINITION_STATUS_ID 900000000000074008 SNOMEDCT_US
DX 19660101 MSH
EFFECTIVE_TIME 20020131 SNOMEDCT_US
MDA 19990101 MSH
MESH_DEFINITION Anemia characterized by appearance of immature myeloid and nucleated erythrocytes in the peripheral blood, resulting from infiltration of the bone marrow by foreign or abnormal tissue. NDFRT
MESH_DUI D000750 NDFRT
MESH_NAME Anemia, Myelophthisic NDFRT
MESH_UI M0001135 NDFRT
MMR 19910613 MSH
MN C15.378.071.307 MSH
MN C15.378.190.636.085 MSH
NDFRT_KIND DISEASE_KIND NDFRT
NUI N0000000394 NDFRT
PRIMARY_PATH 10024383$10028578$10018865$10029104$Leukoerythroblastosis$Myeloproliferative disorders (excl leukaemias)$Haematopoietic neoplasms (excl leukaemias and lymphomas)$Neoplasms benign, malignant and unspecified (incl cysts and polyps) MDR
PRIMARY_PATH 10053199$10002067$10002086$10005329$Leukoerythroblastic anaemia$Anaemias NEC$Anaemias nonhaemolytic and marrow depression$Blood and lymphatic system disorders MDR
PRIMARY_SOC 10005329 MDR
PRIMARY_SOC 10029104 MDR
PT_IN_VERSION 10.0 MDR
PT_IN_VERSION 10.1 MDR
PT_IN_VERSION 11.0 MDR
PT_IN_VERSION 11.1 MDR
PT_IN_VERSION 12.0 MDR
PT_IN_VERSION 12.1 MDR
PT_IN_VERSION 13.0 MDR
PT_IN_VERSION 13.1 MDR
PT_IN_VERSION 14.0 MDR
PT_IN_VERSION 14.1 MDR
PT_IN_VERSION 15.0 MDR
PT_IN_VERSION 15.1 MDR
PT_IN_VERSION 16.0 MDR
PT_IN_VERSION 16.1 MDR
PT_IN_VERSION 17.0 MDR
PT_IN_VERSION 17.1 MDR
PT_IN_VERSION 18.0 MDR
PT_IN_VERSION 18.1 MDR
PT_IN_VERSION 19.0 MDR
PT_IN_VERSION 19.1 MDR
PT_IN_VERSION 20.0 MDR
PT_IN_VERSION 20.1 MDR
PT_IN_VERSION 8.0 MDR
PT_IN_VERSION 8.1 MDR
PT_IN_VERSION 9.0 MDR
PT_IN_VERSION 9.1 MDR
RXAUI 3108976 RXNORM
RXAUI 3108983 RXNORM
RXAUI 3108984 RXNORM
RXCUI 1024889 RXNORM
SMQ_TERM_ADDVERSION 10.0 MDR
SMQ_TERM_ADDVERSION 16.1 MDR
SMQ_TERM_ADDVERSION 8.1 MDR
SMQ_TERM_CAT A MDR
SMQ_TERM_LEVEL 4 MDR
SMQ_TERM_LEVEL 5 MDR
SMQ_TERM_LMVERSION 14.0 MDR
SMQ_TERM_LMVERSION 16.1 MDR
SMQ_TERM_LMVERSION 8.1 MDR
SMQ_TERM_SCOPE 1 MDR
SMQ_TERM_SCOPE 2 MDR
SMQ_TERM_STATUS A MDR
SMQ_TERM_STATUS I MDR
SMQ_TERM_WEIGHT 0 MDR
SNOMED_CID 2694001 NDFRT
SUBSET_MEMBER 447562003~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS D61.9 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPTARGET~D61.9 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS D61.82 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~D61.82 SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~D21y2 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
TERMUI T002241 MSH
TERMUI T002242 MSH
TH NLM (1966) MSH
TH UNK (19XX) MSH
TYPE_ID 900000000000003001 SNOMEDCT_US
TYPE_ID 900000000000013009 SNOMEDCT_US

Additional Concept Data:  (none)

URL to Bookmark: https://ncim-stage.nci.nih.gov/ncimbrowser/ConceptReport.jsp?dictionary=NCI Metathesaurus&code=C0002890

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