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Iron deficiency anemia (CUI C0162316) Suggest changes to this concept
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Terms & Properties

Concept Unique Identifier (CUI): C0162316

NCI Thesaurus Code: C84484  (see NCI Thesaurus info)

Semantic Type: Disease or Syndrome

NCIt Definition: Anemia caused by low iron intake, inefficient iron absorption in the gastrointestinal tract, or chronic blood loss.

NICHD Definition: Anemia caused by inadequate bioavailable iron.

MSH Definition: Anemia characterized by decreased or absent iron stores, low serum iron concentration, low transferrin saturation, and low hemoglobin concentration or hematocrit value. The erythrocytes are hypochromic and microcytic and the iron binding capacity is increased.

Synonyms & Abbreviations: (see Synonym Details)
Anaemia iron deficiency
ANEMIA IRON DEFICIENCY
ANEMIA IRON DEFIC
ANEMIA, IRON DEFICIENCY
Anemia, Iron-Deficiency [Disease/Finding]
Anemia, Iron-Deficiency
ANEMIAS IRON DEFIC
Anemias, Iron Deficiency
Anemias, Iron-Deficiency
Fe deficiency anemia NOS
Ferropenic anaemia
ferropenic anemia
Ferropenic
hypoferric anemia
IDA - Iron deficiency anaemia
IDA - Iron deficiency anemia
Iron def anaemia
Iron def anemia
Iron defic anemia NOS
IRON DEFIC ANEMIAS
IRON DEFIC ANEMIA
Iron deficiency anaemia syndrome
Iron deficiency anaemia, unspecified
Iron deficiency anaemias
Iron deficiency anaemia
Iron deficiency anemia (disorder)
Iron deficiency anemia NOS
Iron deficiency anemia syndrome
Iron deficiency anemia, unspecified
Iron deficiency anemias
iron deficiency anemia
Iron-Deficiency Anemias
Iron-deficiency anemia
Sideropenic anaemia
sideropenic anemia

External Source Codes: 
NCI Thesaurus Code C84484 (see NCI Thesaurus info)

Other Properties: Property Definitions
Name Value Source
ACTIVE 1 SNOMEDCT_US
AN DF: ANEMIA IRON DEFIC MSH
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 900000000000017005 SNOMEDCT_US
CASE_SIGNIFICANCE_ID 900000000000020002 SNOMEDCT_US
CHARACTERISTIC_TYPE_ID 900000000000011006 SNOMEDCT_US
Contributing_Source NICHD NCI
CTV3ID XE13c SNOMEDCT_US
DC 1 MSH
DEFINITION_STATUS_ID 900000000000074008 SNOMEDCT_US
DID 0427-2389 CSP
DX 19950101 MSH
EFFECTIVE_TIME 20020131 SNOMEDCT_US
HN 95; IRON DEFICIENCY ANEMIA was see ANEMIA, HYPOCHROMIC 1970-94 MSH
HN ETOH descriptor 2000. AOD
IAN DEFAULT ICD10
ICE Anemia: {achlorhydric; chlorotic; idiopathic hypochromic; iron [Fe] deficiency NOS} ICD9CM
INCLUSION_TERM anaemia: asiderotic ICD10
INCLUSION_TERM anaemia: hypochromic ICD10
IPX D50 ICPC
MDA 19940531 MSH
MESH_DEFINITION Anemia characterized by decreased or absent iron stores, low serum iron concentration, low transferrin saturation, and low hemoglobin concentration or hematocrit value. The erythrocytes are hypochromic and microcytic and the iron binding capacity is increased. NDFRT
MESH_DUI D018798 NDFRT
MESH_NAME Anemia, Iron-Deficiency NDFRT
MESH_UI M0028144 NDFRT
MMR 19991103 MSH
MN C15.378.071.196.300 MSH
MN C18.452.565.100 MSH
MODIFIER_ID 900000000000451002 SNOMEDCT_US
NDFRT_KIND DISEASE_KIND NDFRT
NICHD_Hierarchy_Term Iron-Deficiency Anemia NCI
NUI N0000003859 NDFRT
OL use ANEMIA, HYPOCHROMIC to search IRON DEFICIENCY ANEMIA 1970-94 MSH
ORDER_NO 03333 ICD10CM
ORDER_NO 03337 ICD10CM
PM 95; IRON DEFICIENCY ANEMIA was see ANEMIA, HYPOCHROMIC 1970-94 MSH
PRIMARY_PATH 10022972$10002042$10002086$10005329$Iron deficiency anaemia$Anaemia deficiencies$Anaemias nonhaemolytic and marrow depression$Blood and lymphatic system disorders MDR
PRIMARY_SOC 10005329 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 8.0 MDR
PT_IN_VERSION 8.1 MDR
PT_IN_VERSION 9.0 MDR
PT_IN_VERSION 9.1 MDR
REF orcid.org/0000-0001-6908-9849 HPO
RXAUI 3108974 RXNORM
RXAUI 3108975 RXNORM
RXAUI 3109013 RXNORM
RXAUI 3183045 RXNORM
RXAUI 3183046 RXNORM
RXCUI 1022877 RXNORM
SNOMED_CID 191133000 NDFRT
SNOMED_CID 87522002 NDFRT
SNOMEDID DC-13010 SNOMEDCT_US
SOS Excludes: familial microcytic anemia (282.49) ICD9CM
SOS Includes: anemia: {asiderotic; hypochromic-microcytic; sideropenic} ICD9CM
SUBSET_MEMBER 447562003~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS D50.9 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~D50.9 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS D50.9 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~IF IRON DEFICIENCY ANEMIA DUE TO DIETARY CAUSES CHOOSE D50.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~IF IRON DEFICIENCY ANEMIA IN MOTHER COMPLICATING CHILDBIRTH CHOOSE D50.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~IF IRON DEFICIENCY ANEMIA IN MOTHER COMPLICATING CHILDBIRTH CHOOSE O99.02 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~IF IRON DEFICIENCY ANEMIA OF PREGNANCY CHOOSE O99.019 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | CONSIDER TRIMESTER SPECIFICATION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~IF IRON DEFICIENCY ANEMIA SECONDARY TO INADEQUATE DIETARY IRON INTAKE CHOOSE D50.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~IF PLUMMER-VINSON SYNDROME CHOOSE D50.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~IF SIDEROPENIC ANEMIA WITH RETICULOENDOTHELIAL SIDEROSIS CHOOSE D50.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~IF SIDEROPENIC ANEMIA WITH RETICULOENDOTHELIAL SIDEROSIS CHOOSE D75.89 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447638001 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447639009 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPGROUP~2 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~2 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~3 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~4 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~5 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~6 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~7 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~IFA 10812081000119108 | Iron deficiency anemia in mother complicating childbirth (disorder) | SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~IFA 191128004 | Iron deficiency anemia due to dietary causes (disorder) | SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~IFA 199248002 | Iron deficiency anemia of pregnancy (disorder) | SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~IFA 290246007 | Sideropenic anemia with reticuloendothelial siderosis (disorder) | SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~IFA 371315009 | Iron deficiency anemia secondary to inadequate dietary iron intake (disorder) | SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~IFA 80126007 | Plummer-Vinson syndrome (disorder) | SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~OTHERWISE TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~D50.1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~D50.8 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~D50.9 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~D75.89 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~O99.019 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~O99.02 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~ SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~XE13c SNOMEDCT_US
SUBSET_MEMBER 900000000000498005~MAPTARGET~DC-13010 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 T055999 MSH
TERMUI T056000 MSH
TERMUI T056001 MSH
TERMUI T056002 MSH
TH NLM (1995) 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=C0162316

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