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Term connections

RelationshipRelates toConcept idVocabulary
Active possibly_equivalent_to inactive (SNOMED)
Dipstick assessment of hemoglobin concentration
4121316
SNOMED
Hemoglobin determination
4148063
SNOMED
Associated procedure of (SNOMED)
Hemoglobin requested
4013399
SNOMED
Has Module
SNOMED CT core
40642539
SNOMED
Has component
Hemoglobin
4244232
SNOMED
Has method
Measurement - action
4044177
SNOMED
Has status
Primitive
40642538
SNOMED
Interprets of (SNOMED)
A-gamma beta+ HPFH AND beta0 thalassemia in cis
4242755
SNOMED
AMeD syndrome
1075863
SNOMED
Aase syndrome
4217370
SNOMED
Achlorhydric anemia
4213893
SNOMED
Acquired aplastic anemia
4184758
SNOMED
Acquired hemoglobin H disease
4139556
SNOMED
Acquired iron deficiency anemia due to decreased absorption
37110336
SNOMED
Acquired iron deficiency anemia due to increased iron requirement
36713573
SNOMED
Acquired pancytopenia
4239484
SNOMED
Acquired red cell aplasia
138723
SNOMED
Acquired thiamine deficiency anemia
36715580
SNOMED
Acquired thrombotic thrombocytopenic purpura
4204900
SNOMED
Acute megaloblastic anemia due to dialysis
4097961
SNOMED
Acute sickle cell splenic sequestration crisis
40485018
SNOMED
Acute splenic sequestration due to sickle cell hemoglobin C disease with crisis
603018
SNOMED
Acute splenic sequestration of spleen due to sickle cell thalassemia with crisis
607430
SNOMED
Adult pure red cell aplasia
35623407
SNOMED
Agamma delta beta0 thalassemia
4232474
SNOMED
Alpha plus thalassemia
4271753
SNOMED
Alpha plus thalassemia deletion type
4311397
SNOMED
Alpha plus thalassemia non deletion type
4311538
SNOMED
Alpha thalassemia
4287844
SNOMED
Alpha thalassemia X-linked intellectual disability syndrome
37399441
SNOMED
Alpha thalassemia-2 trait
4121113
SNOMED
Alpha thalassemia-mental retardation syndrome
4080702
SNOMED
Alpha trait thalassemia
4098749
SNOMED
Alpha zero thalassemia
4278816
SNOMED
Alpha-beta thalassemia
4122931
SNOMED
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16
42539413
SNOMED
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome
36715351
SNOMED
Amino acid deficiency anemia
4276524
SNOMED
Anemia caused by antineoplastic agent
608596
SNOMED
Anemia caused by heat
4185253
SNOMED
Anemia caused by lead
4278920
SNOMED
Anemia caused by zidovudine
37018722
SNOMED
Anemia co-occurrent with human immunodeficiency virus infection
37017132
SNOMED
Anemia due to chemotherapy
4178792
SNOMED
Anemia due to disturbance of hemoglobin synthesis
4031662
SNOMED
Anemia due to nuclear maturation defect
42596489
SNOMED Veterinary
Anemia due to substance
4312008
SNOMED
Anemia during pregnancy - baby delivered
432968
SNOMED
Anemia during pregnancy - baby not yet delivered
432967
SNOMED
Anemia in chronic kidney disease stage 4
37398911
SNOMED
Anemia in chronic kidney disease stage 5
37395652
SNOMED
Anemia in the puerperium - baby delivered during current episode of care
442923
SNOMED
Anemia in the puerperium - baby delivered during previous episode of care
442922
SNOMED
Anemia of prematurity
432452
SNOMED
Anemia secondary to hookworm infestation
42596486
SNOMED Veterinary
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent
37017607
SNOMED
Aplastic anemia
137829
SNOMED
Aplastic anemia associated with metabolic alteration
4186108
SNOMED
Aplastic anemia associated with pancreatitis
4211348
SNOMED
Aplastic anemia associated with pregnancy
4187773
SNOMED
Aplastic anemia caused by antineoplastic agent
37016151
SNOMED
Aplastic anemia caused by toxic cause
4100998
SNOMED
Aplastic anemia co-occurrent with human immunodeficiency virus infection
37019055
SNOMED
Aplastic anemia due to chronic disease
4101582
SNOMED
Aplastic anemia due to drugs
4146088
SNOMED
Aplastic anemia due to infection
4101583
SNOMED
Aplastic anemia due to radiation
4098027
SNOMED
Aplastic anemia with AIDS (acquired immunodeficiency syndrome)
4225810
SNOMED
Aregenerative anemia
4230471
SNOMED
Ataxia pancytopenia syndrome
35625536
SNOMED
Atypical hemolytic uremic syndrome
37312165
SNOMED
Atypical hemolytic uremic syndrome with anti-factor H antibodies
1244954
SNOMED
Atypical hemolytic uremic syndrome with complement gene abnormality
1244936
SNOMED
Atypical isoimmunization of newborn
4173192
SNOMED
Autoimmune pancytopenia
4082738
SNOMED
Autoimmune thrombotic thrombocytopenic purpura
4230266
SNOMED
Beta plus thalassemia
4196206
SNOMED
Beta plus thalassemia normal hemoglobin A-2 type 1 silent
4187256
SNOMED
Beta thalassemia
4278669
SNOMED
Beta thalassemia X-linked thrombocytopenia syndrome
37397537
SNOMED
Beta thalassemia intermedia
4100992
SNOMED
Beta thalassemia trait
4149681
SNOMED
Beta zero thalassemia
4315393
SNOMED
Beta zero thalassemia deletion type
4099005
SNOMED
Beta zero thalassemia non deletion type
4009304
SNOMED
Cellular immunologic aplastic anemia
4177177
SNOMED
Central nervous system calcification, deafness, tubular acidosis, anemia syndrome
37111627
SNOMED
Chicken anaemia virus infection
42599372
SNOMED Veterinary
Chronic acquired pure red cell aplasia
4234973
SNOMED
Chronic idiopathic autoimmune hemolytic anemia
4318674
SNOMED
Chronic idiopathic thrombocytopenic purpura
318397
SNOMED
Congenital anemia
434156
SNOMED
Congenital atransferrinemia
4009784
SNOMED
Congenital dyserythropoietic anemia
4204062
SNOMED
Congenital dyserythropoietic anemia type IV
36714288
SNOMED
Congenital dyserythropoietic anemia, type I
4241982
SNOMED
Congenital dyserythropoietic anemia, type II
4286660
SNOMED
Congenital dyserythropoietic anemia, type III
4097214
SNOMED
Congenital hemolytic anemia
4175331
SNOMED
Congenital hemolytic uremic syndrome
40481595
SNOMED
Congenital hypoplastic anemia
4228194
SNOMED
Congenital megaloblastic anemia due to transcobalamin II deficiency
606065
SNOMED
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism
4178677
SNOMED
Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome
35623048
SNOMED
Congenital thrombocytopenic purpura
437242
SNOMED
Congenital transferrin deficiency
4121107
SNOMED
Constitutional aplastic anemia
140681
SNOMED
Constitutional aplastic anemia with malformation
4146086
SNOMED
Delta beta thalassemia
4038772
SNOMED
Delta beta thalassemia trait
1245854
SNOMED
Delta beta zero thalassemia
4297017
SNOMED
Delta thalassemia
4039785
SNOMED
Delta zero thalassemia
4267282
SNOMED
Delta-beta-Lepore thalassemia
4122930
SNOMED
Diarrhea-associated hemolytic uremic syndrome
4190190
SNOMED
Diarrhea-negative hemolytic uremic syndrome
4159967
SNOMED
Doan-Wright syndrome
4305588
SNOMED
Dominant beta-thalassemia
37396761
SNOMED
Drug induced thrombotic thrombocytopenic purpura
4258261
SNOMED
Drug-induced immune hemolytic anemia
4131918
SNOMED
Duffy isoimmunization of the newborn
4139551
SNOMED
Epsilon gamma delta beta thalassemia
4052711
SNOMED
Epsilon gamma delta beta0 thalassemia
4248254
SNOMED
Erythrogenesis imperfecta
4101581
SNOMED
Estren-Dameshek anemia
4188208
SNOMED
Familial hemolytic uremic syndrome
36717581
SNOMED
Familial megaloblastic anemia
4235788
SNOMED
Fanconi anemia of complementation group C
37168560
SNOMED
Fanconi's anemia
4148471
SNOMED
Feline infectious anaemia
42572621
SNOMED Veterinary
Flea bite anemia
42596091
SNOMED Veterinary
Gamma delta beta thalassemia
37311954
SNOMED
Gamma thalassemia
4122932
SNOMED
Ghosal hematodiaphyseal dysplasia
4308062
SNOMED
Glutathione synthase deficiency with 5-oxoprolinuria
4192278
SNOMED
Glutathione synthase deficiency without 5-oxoprolinuria
4035266
SNOMED
Glutathione synthetase deficiency
4121287
SNOMED
HNSHA (hereditary nonspherocytic hemolytic anemia) due to pyruvate kinase deficiency
4254249
SNOMED
HNSHA due to NADH diaphorase deficiency
4171026
SNOMED
HNSHA due to NADH-methemoglobin reductase deficiency
4320919
SNOMED
HNSHA due to aldolase A deficiency
4009787
SNOMED
HNSHA due to decreased adenosine deaminase activity
4193514
SNOMED
HNSHA due to diphosphoglycerate mutase deficiency
4265915
SNOMED
HNSHA due to gamma glutamyl cysteine synthetase deficiency
4101917
SNOMED
HNSHA due to glucose phosphate isomerase deficiency
4181143
SNOMED
HNSHA due to glutathione reductase deficiency
4178731
SNOMED
HNSHA due to glutathione synthetase deficiency
4009788
SNOMED
HNSHA due to hexokinase deficiency
4174701
SNOMED
HNSHA due to phosphofructokinase deficiency
4187034
SNOMED
HNSHA due to phosphoglycerate kinase deficiency
4242111
SNOMED
HNSHA due to pyrimidine-5'-nucleotidase deficiency
4145277
SNOMED
HNSHA due to triosephosphate isomerase deficiency
4258685
SNOMED
HPFH A gamma beta+ thalassemia
4213820
SNOMED
HPFH deletion type
4311673
SNOMED
HPFH linked to beta-globulin gene cluster
4231453
SNOMED
HPFH nondeletion type
4206913
SNOMED
HPFH unlinked to beta-globulin gene cluster
4140101
SNOMED
Hb Lepore thalassemia
4290233
SNOMED
HbE (haemoglobin E) beta plus thalassaemia
3657472
SNOMED
HbE (haemoglobin E) beta zero thalassaemia
3657471
SNOMED
Hematopoietic subsyndrome of acute radiation syndrome
37109690
SNOMED
Hemoglobin Bart's hydrops syndrome
4200254
SNOMED
Hemoglobin C beta plus thalassemia
1246707
SNOMED
Hemoglobin C beta zero thalassemia
1246708
SNOMED
Hemoglobin C/beta thalassemia disease
760845
SNOMED
Hemoglobin Constant Spring trait
4125628
SNOMED
Hemoglobin D beta plus thalassemia
1246709
SNOMED
Hemoglobin D beta zero thalassemia
1246710
SNOMED
Hemoglobin D/beta thalassemia disease
765176
SNOMED
Hemoglobin E beta plus thalassemia
1246711
SNOMED
Hemoglobin E beta zero thalassemia
1246712
SNOMED
Hemoglobin E/beta thalassemia disease
4120455
SNOMED
Hemoglobin H constant spring thalassemia
40491316
SNOMED
Hemoglobin H disease
4168911
SNOMED
Hemoglobin Lepore trait
4121114
SNOMED
Hemoglobin Paksé disease
602960
SNOMED
Hemoglobin SS disease with crisis
26942
SNOMED
Hemoglobin SS disease with vasoocclusive crisis
4209085
SNOMED
Hemoglobin SS disease without crisis
30683
SNOMED
Hemoglobin Seal Rock disease
606952
SNOMED
Hemoglobin above reference range
4038953
SNOMED
Hemoglobin below reference range
4013074
SNOMED
Hemoglobin borderline high
4013075
SNOMED
Hemoglobin borderline low
4013401
SNOMED
Hemoglobin finding
4094758
SNOMED
Hemoglobin level outside reference range
40480513
SNOMED
Hemoglobin very high
4013837
SNOMED
Hemoglobin very low
4013073
SNOMED
Hemoglobin within reference range
4013836
SNOMED
Hemolytic anemia associated with chronic inflammatory disease
4077896
SNOMED
Hemolytic anemia associated with lymphoproliferative disorder
4281372
SNOMED
Hemolytic anemia associated with rheumatic disorder
4009790
SNOMED
Hemolytic anemia associated with systemic lupus erythematosus
4320480
SNOMED
Hemolytic anemia associated with ulcerative colitis
4005188
SNOMED
Hemolytic anemia due to adenylate kinase deficiency
35624317
SNOMED
Hemolytic anemia due to erythrocyte adenosine deaminase overproduction
4203291
SNOMED
Hemolytic anemia due to glutathione metabolism disorder
23988
SNOMED
Hemolytic anemia due to pyruvate kinase deficiency
4098746
SNOMED
Hemolytic anemia due to triose phosphate isomerase deficiency
4100991
SNOMED
Hemolytic anemia of pregnancy
606061
SNOMED
Hemolytic disease of fetus OR newborn due to ABO immunization
437090
SNOMED
Hemolytic disease of fetus OR newborn due to RhD isoimmunization
433603
SNOMED
Hemolytic disease of fetus OR newborn due to isoimmunization
440218
SNOMED
Hemolytic disease of fetus due to ABO immunization
601103
SNOMED
Hemolytic disease of newborn co-occurrent and due to ABO immunization
36713168
SNOMED
Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization
4009645
SNOMED
Hemolytic uremic syndrome
197253
SNOMED
Hemolytic uremic syndrome of childhood
4267646
SNOMED
Hemolytic uremic syndrome with DGKE deficiency
37167956
SNOMED
Hemolytic uremic syndrome, adult type
4302298
SNOMED
Hereditary cryohydrocytosis with normal stomatin
36676579
SNOMED
Hereditary cryohydrocytosis with reduced stomatin
37204308
SNOMED
Hereditary elliptocytosis
22288
SNOMED
Hereditary elliptocytosis due to abnormal protein 4.1
4327824
SNOMED
Hereditary elliptocytosis due to alpha spectrin defect
4228681
SNOMED
Hereditary elliptocytosis due to beta spectrin defect in self-association
4218794
SNOMED
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction
4281394
SNOMED
Hereditary elliptocytosis due to deficiency of protein 4.1
4243676
SNOMED
Hereditary elliptocytosis due to glycophorin C deficiency
4034711
SNOMED
Hereditary elliptocytosis with transient poikilocytosis
4125633
SNOMED
Hereditary folate deficiency anemia
42536531
SNOMED
Hereditary hemolytic anemia
28396
SNOMED
Hereditary iron deficiency anemia
607422
SNOMED
Hereditary isolated aplastic anemia
37204551
SNOMED
Hereditary nonspherocytic hemolytic anemia
4115393
SNOMED
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia
4264017
SNOMED
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia
4203904
SNOMED
Hereditary persistence of fetal hemoglobin thalassemia
4061151
SNOMED
Hereditary sideroblastic anemia
4269075
SNOMED
Hereditary spherocytosis
24909
SNOMED
Hereditary spherocytosis due to beta spectrin defect
4320651
SNOMED
Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
4168441
SNOMED
Hereditary spherocytosis due to deficiency of protein 4.2
4144956
SNOMED
Hereditary spherocytosis due to spectrin deficiency
4099224
SNOMED
Hereditary stomatocytosis
4031827
SNOMED
Hereditary vitamin B12 deficiency anemia
42536530
SNOMED
Heterozygous thalassemia
4023612
SNOMED
Homozygous alpha thalassemia
4120454
SNOMED
Homozygous beta thalassemia
4132431
SNOMED
Homozygous hemoglobin H constant spring thalassemia
760844
SNOMED
Homozygous hereditary elliptocytosis
607421
SNOMED
Humoral immunologic aplastic anemia
4031699
SNOMED
Hypochromic microcytic anemia with iron overload
46272744
SNOMED
Hypoplastic anemia
4218974
SNOMED
Idiopathic aplastic anemia
4098145
SNOMED
Idiopathic chronic cold agglutinin disease
4273847
SNOMED
Idiopathic paroxysmal cold hemoglobinuria
4271197
SNOMED
Idiopathic sideroblastic anemia
4173028
SNOMED
Immunologic aplastic anemia
4298690
SNOMED
Infection-related hemolytic uremic syndrome
37167983
SNOMED
Infectious avian anaemia
42599242
SNOMED Veterinary
Iron deficiency anemia
436659
SNOMED
Iron deficiency anemia due to blood loss
37119138
SNOMED
Iron deficiency anemia due to celiac disease
606928
SNOMED
Iron deficiency anemia due to dietary causes
4100985
SNOMED
Iron deficiency anemia due to increased requirement in adolescence
606923
SNOMED
Iron deficiency anemia due to increased requirement in infancy
606924
SNOMED
Iron deficiency anemia during maternal intrapartum period
1244473
SNOMED
Iron deficiency anemia in mother complicating childbirth
45772084
SNOMED
Iron deficiency anemia of pregnancy
4058246
SNOMED
Iron deficiency anemia secondary to inadequate dietary iron intake
433168
SNOMED
Iron-refractory iron deficiency anemia
36716126
SNOMED
Juvenile type megaloblastic anemia
4171201
SNOMED
Kell isoimmunization of the newborn
4122929
SNOMED
Kidd isoimmunization of the newborn
4139552
SNOMED
Late anemia due to isoimmunization
436820
SNOMED
Late anemia of newborn
4173191
SNOMED
Late anemia of newborn due to isoimmunization
4071073
SNOMED
Lethal hemolytic anemia and genital anomaly syndrome
36714258
SNOMED
Macrocytic anemia of pregnancy
606052
SNOMED
Macrocytic hypochromic anemia
42596487
SNOMED Veterinary
Macrocytic normochromic anemia
42596488
SNOMED Veterinary
Majeed syndrome
45766392
SNOMED
Mechanical hemolysis following insertion of prosthetic heart valve
600662
SNOMED
Megaloblastic anemia due to alcoholism
4338370
SNOMED
Megaloblastic anemia due to blind loop syndrome
4243950
SNOMED
Megaloblastic anemia due to celiac disease
4282785
SNOMED
Megaloblastic anemia due to congenital deficiency of intrinsic factor
4247416
SNOMED
Megaloblastic anemia due to disease of small intestine
4221567
SNOMED
Megaloblastic anemia due to error of cobalamin metabolism
4287574
SNOMED
Megaloblastic anemia due to error of folate metabolism
4149183
SNOMED
Megaloblastic anemia due to folate deficiency due to increased requirement
36715492
SNOMED
Megaloblastic anemia due to folate deficiency in pregnancy and lactation
36715493
SNOMED
Megaloblastic anemia due to folate deficiency in prematurity
36715494
SNOMED
Megaloblastic anemia due to impaired absorption of folate
4100962
SNOMED
Megaloblastic anemia due to inborn errors of metabolism
4147911
SNOMED
Megaloblastic anemia due to pregnancy
4238731
SNOMED
Megaloblastic anemia due to tropical sprue
4338976
SNOMED
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness
4034963
SNOMED
Microangiopathic hemolytic anemia
4198102
SNOMED
Microcytic anemia
4121106
SNOMED
Microcytic hypochromic anemia
4262948
SNOMED
Microcytic normochromic anemia
4172446
SNOMED
Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
4093515
SNOMED
Mild hereditary spherocytosis due to spectrin deficiency
4138560
SNOMED
Mitochondrial myopathy with sideroblastic anemia syndrome
37110070
SNOMED
Neonatal anemia
4339722
SNOMED
Neonatal autoimmune hemolytic anemia
36674478
SNOMED
Nonregenerative anemia
954172
SNOMED Veterinary
Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase
37110727
SNOMED
Nutritional anemia of pregnancy
606027
SNOMED
O/E - clinically anemic
4062928
SNOMED
O/E - equivocally anemic
4063215
SNOMED
O/E - profoundly anemic
4063216
SNOMED
Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome
36716259
SNOMED
Pancytopenia
432881
SNOMED
Pancytopenia caused by anticonvulsant
601067
SNOMED
Pancytopenia caused by antidiabetic drug
1077005
SNOMED
Pancytopenia caused by antithyroid drug
601066
SNOMED
Pancytopenia caused by colchicine
1246248
SNOMED
Pancytopenia caused by immunosuppressant
37209558
SNOMED
Pancytopenia caused by medication
42536958
SNOMED
Pancytopenia caused by non-steroidal anti-inflammatory agent
1246249
SNOMED
Pancytopenia due to IKZF1 mutations
37204478
SNOMED
Pancytopenia due to antineoplastic chemotherapy
36713112
SNOMED
Pancytopenia with developmental delay syndrome
36674474
SNOMED
Pancytopenia with pancreatitis
4125494
SNOMED
Pancytopenia-dysmelia
4077348
SNOMED
Parvoviral aplastic crisis
4345236
SNOMED
Perinatal anemia
4306199
SNOMED
Pernicious anemia due to autoimmune disorder
603007
SNOMED
Physiological anemia of infancy
4079852
SNOMED
Plummer-Vinson syndrome
4198185
SNOMED
Post gastrectomy iron deficiency anemia
606921
SNOMED
Post infectious thrombocytopenic purpura
4140545
SNOMED
Postpartum iron deficiency anemia
1244157
SNOMED
Posttransfusion purpura
4247776
SNOMED
Primaquine sensitivity anemia
3661615
SNOMED
Primary (idiopathic) autoimmune hemolytic anemia
4131915
SNOMED
Primary (idiopathic) warm autoimmune hemolytic anemia
4130679
SNOMED
Primary CD59 deficiency
36674519
SNOMED
Protein-deficiency anemia
436083
SNOMED
Pure red cell aplasia, acquired
4125496
SNOMED
Refractory anemia (clinical)
4003185
SNOMED
Refractory anemia with excess blasts in transformation (clinical)
4002495
SNOMED
Refractory anemia without sideroblasts, so stated
4099508
SNOMED
Revesz syndrome
37117164
SNOMED
Rhesus isoimmunization due to anti-Cw
4139550
SNOMED
Rhesus isoimmunization due to anti-D
4145893
SNOMED
Rhesus isoimmunization due to anti-E
4143895
SNOMED
Rhesus isoimmunization due to anti-c
4139549
SNOMED
Secondary aplastic anemia
4184200
SNOMED
Secondary sideroblastic anemia due to drugs and toxins
4101000
SNOMED
Selective malabsorption of cyanocobalamin
4121110
SNOMED
Severe combined immunodeficiency with reticular dysgenesis
4097998
SNOMED
Severe congenital hypochromic anemia with ringed sideroblasts
37110923
SNOMED
Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
4021466
SNOMED
Severe hereditary spherocytosis due to spectrin deficiency
4298813
SNOMED
Sickle cell anemia in mother complicating childbirth
45757146
SNOMED
Sickle cell anemia with coexistent alpha-thalassemia
4131914
SNOMED
Sickle cell anemia with high hemoglobin F
4121115
SNOMED
Sickle cell beta plus thalassemia
4130678
SNOMED
Sickle cell trait with coexistent alpha-thalassemia
4130189
SNOMED
Sickle cell-beta-thalassemia
4130067
SNOMED
Sickle cell-beta0-thalassemia
4130068
SNOMED
Sickle cell-delta beta0-thalassemia
4131913
SNOMED
Sickle cell-hemoglobin SS disease
22281
SNOMED
Sickle cell-thalassemia disease
315523
SNOMED
Sickle cell-thalassemia disease with crisis
443738
SNOMED
Sickle cell-thalassemia disease without crisis
321263
SNOMED
Sideropenic anemia with reticuloendothelial siderosis
4157495
SNOMED
Thalassemia
30978
SNOMED
Thalassemia in mother complicating childbirth
45757189
SNOMED
Thalassemia in mother complicating pregnancy
45773071
SNOMED
Thalassemia intermedia
4247579
SNOMED
Thalassemia major
4327045
SNOMED
Thalassemia syndrome
4222774
SNOMED
Thalassemia with other hemoglobinopathy
4188474
SNOMED
Thalassemia-hemoglobin C disease
4264909
SNOMED
Thiamine-responsive megaloblastic anemia
4044728
SNOMED
Thrombocytopenic purpura
4119134
SNOMED
Thrombocytopenic purpura associated with metabolic disorder
4214947
SNOMED
Thrombocytopenic purpura due to defective platelet production
4299560
SNOMED
Thrombocytopenic purpura due to platelet consumption
4292531
SNOMED
Thrombotic thrombocytopenic purpura
4301602
SNOMED
Transient acquired pure red cell aplasia
4098028
SNOMED
Transient hypoplastic anemia
4098760
SNOMED
Unstable hemoglobin disease
4082253
SNOMED
Upshaw-Schulman syndrome
4159966
SNOMED
Vitamin B12 deficiency anemia due to chronic atrophic gastritis
607426
SNOMED
Vitamin B12 deficiency anemia following gastrectomy
37160905
SNOMED
Vitamin B12 deficiency anemia following total gastrectomy
603011
SNOMED
WT limb blood syndrome
36713970
SNOMED
X chromosome-linked pyridoxine refractory sideroblastic anemia
4060269
SNOMED
X chromosome-linked pyridoxine responsive sideroblastic anemia
4102056
SNOMED
X chromosome-linked sideroblastic anemia
40599994
SNOMED
X-linked congenital dyserythropoietic anemia with thrombocytopenia
36716460
SNOMED
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia
37204236
SNOMED
X-linked sideroblastic anemia with spinocerebellar ataxia
36714533
SNOMED
[X]Aplastic and other anaemias
44794611
SNOMED
[X]Haemolytic anaemias
44796118
SNOMED
beta+ Thalassemia normal Hb A-2 type 2
4035988
SNOMED
Is a
Hematology test
4090979
SNOMED
Protein measurement
4250176
SNOMED
Red blood cell test
4098353
SNOMED
Non-standard to Standard map (OMOP)
Measurement of total hemoglobin concentration
40480067
SNOMED
SNOMED to CPT-4 equivalent (OMOP)
Blood count; hemoglobin (Hgb)
2212643
CPT4
Blood count; reticulocytes, automated, including 1 or more cellular parameters (eg, reticulocyte hemoglobin content [CHr], immature reticulocyte fraction [IRF], reticulocyte volume [MRV], RNA content), direct measurement
2212655
CPT4
Hemoglobin level 11 g/dL to 12.9 g/dL (CKD, ESRD)
2106864
CPT4
Hemoglobin level greater than or equal to 13 g/dL (CKD, ESRD)
2106862
CPT4
Hemoglobin level less than 11 g/dL (CKD, ESRD)
2106867
CPT4
Standard to Non-standard map (OMOP)
Decreased Hemoglobin
45929487
CIEL
Decreased haemoglobin
3087355
Nebraska Lexicon
Decreased haemoglobin
3087752
Nebraska Lexicon
Haemoglobin
45937959
CIEL
Haemoglobin Low
45928384
CIEL
Haemoglobin abnormal
45471991
Read
Haemoglobin borderline high
3094860
Nebraska Lexicon
Haemoglobin borderline high
3443161
Nebraska Lexicon
Haemoglobin borderline high
45495203
Read
Haemoglobin borderline low
3094858
Nebraska Lexicon
Haemoglobin borderline low
3436539
Nebraska Lexicon
Haemoglobin borderline low
45458443
Read
Haemoglobin determination
3150088
Nebraska Lexicon
Haemoglobin high
3074624
Nebraska Lexicon
Haemoglobin high
3110743
Nebraska Lexicon
Haemoglobin high
3157669
Nebraska Lexicon
Haemoglobin high
45471990
Read
Haemoglobin level outside reference range
3470413
Nebraska Lexicon
Haemoglobin low
3094857
Nebraska Lexicon
Haemoglobin low
3433488
Nebraska Lexicon
Haemoglobin low
45511824
Read
Haemoglobin normal
3094859
Nebraska Lexicon
Haemoglobin normal
3474420
Nebraska Lexicon
Haemoglobin normal
45468710
Read
Haemoglobin very high
3094862
Nebraska Lexicon
Haemoglobin very high
3444860
Nebraska Lexicon
Haemoglobin very high
45465254
Read
Haemoglobin very low
45435191
Read
Haemoglobin very low
3094856
Nebraska Lexicon
Haemoglobin very low
3459327
Nebraska Lexicon
Hemoglobin
37546133
CDISC
Hemoglobin borderline high
4013075
SNOMED
Hemoglobin borderline high
40301220
SNOMED
Hemoglobin borderline low
4013401
SNOMED
Hemoglobin borderline low
40301218
SNOMED
Hemoglobin high
40301221
SNOMED
Hemoglobin high
40332329
SNOMED
Hemoglobin only
45934950
CIEL
Hemoglobin[Spectrophotometry],Diagnostic and laboratory test qualitative addition(1%)
19682104
EDI
Hemoglobin[Spectrophotometry],Diagnostic and laboratory test qualitative addition(2%)
19682103
EDI
Hemoglobin[Spectrophotometry],Diagnostic and laboratory test qualitative addition(3%)
19682102
EDI
Hemoglobin[Spectrophotometry],Diagnostic and laboratory test qualitative addition(4%)
19682101
EDI
Hemoglobin[Spectrophotometry],Nuclear medicine examination qualitative addition(4%)
19682105
EDI
Hemoglobin[Visual Method],Diagnostic and laboratory test qualitative addition(1%)
19682095
EDI
Hemoglobin[Visual Method],Diagnostic and laboratory test qualitative addition(2%)
19682094
EDI
Hemoglobin[Visual Method],Diagnostic and laboratory test qualitative addition(3%)
19682093
EDI
Hemoglobin[Visual Method],Diagnostic and laboratory test qualitative addition(4%)
19682092
EDI
Hemoglobin[Visual Method],Nuclear medicine examination qualitative addition(4%)
19682096
EDI
Increased haemoglobin
3087354
Nebraska Lexicon
Increased haemoglobin
3459484
Nebraska Lexicon
LOW HAEMOGLOBIN
45531912
OXMIS
Measurement of total haemoglobin concentration
3430766
Nebraska Lexicon
Measurement of total hemoglobin concentration
40480067
SNOMED
Subsumes
Copper sulfate screening test
4097895
SNOMED
Hemoglobin (Hgb), quantitative, transcutaneous
40756996
CPT4
Hemoglobin by copper sulfate method, non-automated
4016938
SNOMED
Measurement of total hemoglobin concentration and hematocrit
4288754
SNOMED
Measurement of total hemoglobin concentration in plasma specimen
4015178
SNOMED
Measurement of total hemoglobin concentration in urine specimen
4016242
SNOMED
Measurement of total hemoglobin concentration using dipstick
40484519
SNOMED
Semi-quantitative measurement of total hemoglobin in blood specimen
4015177
SNOMED
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OMOP Vocabulary version: v20250227

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    1. The sub-licensee is only permitted to access SNOMED CT® using this software (or service) for the purpose of exploring and evaluating the terminology.
    2. The sub-licensee is not permitted the use of this software as part of a system that constitutes a SNOMED CT "Data Creation System" or "Data Analysis System", as defined in the SNOMED International Affiliate License. This means that the sub-licensee must not use SNOMED International SNOMED CT Browser to add or copy SNOMED CT identifiers into any type of record system, database or document.
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  5. SNOMED International Affiliates may use SNOMED International SNOMED CT Browser as part of a "Data Creation System" or "Data Analysis System" subject to the following conditions:
    1. The SNOMED International Affiliate, using SNOMED International SNOMED CT Browsermust accept full responsibility for any reporting and fees due for use or deployment of such a system in a Non-Member Territory.
    2. The SNOMED International Affiliate must not useSNOMED International SNOMED CT Browser to access or interact with SNOMED CT in any way that is not permitted by the Affiliate License Agreement.
    3. In the event of termination of the Affiliate License Agreement, the use ofSNOMED International SNOMED CT Browser will be subject to the End User limitations noted in 4.

HemOnc license agreement

The HemOnc Vocabulary is a derivative product of HemOnc.org, which is wholly owned and operated by HemOnc.org LLC. Use of the HemOnc Vocabulary is governed by the conditions of this License Agreement issued by HemOnc.org LLC:
  1. The meaning of the terms “Data Analysis System”, “Data Creation System”, and “License” is defined below.
  2. If you are already holding a HemOnc ontology License, you are subject to the terms and conditions of the License for the version of the HemOnc Vocabulary which was provided to you. If you wish to obtain this version of the HemOnc Vocabulary, you are subject to the following limitations.
  3. If you currently do not hold a HemOnc ontology License, you may access the HemOnc Vocabulary subject to acceptance of and adherence to the following limitations:
    1. You are permitted to access HemOnc using this software for the purpose of exploring and evaluating the terminology.
    2. You are permitted to use HemOnc as part of a system that constitutes a Data Analysis System, as defined below.
    3. You are not permitted the use of HemOnc as part of a system that constitutes a Data Creation System, as defined below. This means that you must not use HemOnc identifiers in any type of system intended for direct or indirect patient care.
    4. If you share the Licensed Material with a third party, attribution of the HemOnc vocabulary must be given to HemOnc.org LLC, with a URI or hyperlink to HemOnc.org provided if reasonably possible. Use of HemOnc by a third party would be limited to a Data Analysis System and a copy of this License Agreement must be supplied to the third party.
    5. You may not use HemOnc as a substitute for formal medical training, substitute it for independent clinical judgment, and construe it as offering medical advice.

If you wish to utilize the vocabulary for purposes other than specified here, contact us by emailing licensing@hemonc.org.

You agree to indemnify and hold HemOnc.org LLC and all parties who have contributed to HemOnc.org and this derivative product harmless from and against all claims, liability, losses, damages, costs, and expenses, including--but not limited to--legal fees

Definitions

Data Analysis System: a computer system that is used to analyze records or other data, but not if that system is also a Data Creation System

Data Creation System: a computer system that is used to create records or other data that is encoded using HemOnc, for the purposes of facilitating patient care

License: the separate CC BY-NC-SA 4.0 license to the full HemOnc ontology