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441689006: Measurement of total hemoglobin concentration (procedure)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2817597012 Measurement of total haemoglobin concentration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2817598019 Measurement of total hemoglobin concentration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2817599010 Measurement of total hemoglobin concentration (procedure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2312981000195113 Messung der Gesamthämoglobinkonzentration de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

7 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Measurement of total haemoglobin concentration Is a Red blood cell test false Inferred relationship Some
Measurement of total haemoglobin concentration Is a Protein measurement true Inferred relationship Some
Measurement of total haemoglobin concentration Component Erythrocyte (cell) false Inferred relationship Some 3
Measurement of total haemoglobin concentration Component Hemoglobin true Inferred relationship Some 1
Measurement of total haemoglobin concentration Method Measurement - action false Inferred relationship Some 2
Measurement of total haemoglobin concentration Is a Haematology test true Inferred relationship Some
Measurement of total haemoglobin concentration Method Measurement - action true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Autoimmune hemolytic anemia caused by immunoglobulin M Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Acute megaloblastic anemia secondary to total parenteral nutrition Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Anemia caused by arsenic hydride Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Severe hereditary spherocytosis due to spectrin deficiency Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
G-6-PD class V variant anemia Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Hemolytic anemia caused by drugs (disorder) Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
G-6-PD class IV variant anemia Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Anaemia due to diabetes mellitus Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 1
G-6-PD variant enzyme deficiency anemia Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Autoimmune haemolytic anaemia caused by IgA Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Primary (idiopathic) autoimmune hemolytic anemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Chronic cold agglutinin disease Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Autoimmune hemolytic anemia, categorized by antibody class AND/OR complement Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Hemolytic anemia caused by hyperbaric oxygen Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Primary cold-type hemolytic anemia Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Secondary cold-type hemolytic anemia Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Neonatal anemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Maternal autoimmune hemolytic anemia Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Familial megaloblastic anemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Diarrhea-associated hemolytic uremic syndrome (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Perinatal anemia (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Cold autoimmune hemolytic anemia (disorder) Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Autoimmune hemolytic anemia (disorder) Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Acute sickle cell splenic sequestration crisis (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Fetal anemia Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Anaemia in chronic kidney disease Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
A rare syndromic, inherited form of sideroblastic anemia characterized by mild to moderate anemia (with hypochromia and microcytosis) and early-onset, non- or slowly progressive spinocerebellar ataxia. Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 7
Anaemia co-occurrent and due to chronic kidney disease stage 3 Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Microangiopathic hemolytic anemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hereditary spherocytosis Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hemolytic anemia due to triose phosphate isomerase deficiency Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Traumatic hemolytic anemia (disorder) Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Chronic hemolytic anemia (disorder) Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Mixed autoimmune hemolytic anemia is a type of autoimmune hemolytic anemia defined by the presence of both warm and cold autoantibodies, which have a deleterious effect on red blood cells at either body temperature or at lower temperatures. Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 9
Hemolytic anemia associated with chronic inflammatory disease Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Secondary paroxysmal cold hemoglobinuria Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
HNSHA due to glutathione reductase deficiency Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hemolytic anemia associated with lymphoproliferative disorder Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Hemolytic anemia associated with rheumatic disorder Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Sickle cell-hemoglobin SS disease Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Secondary warm autoimmune hemolytic anemia Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Paroxysmal cold hemoglobinuria associated with tertiary syphilis Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Hemolytic anemia due to hexokinase deficiency Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Aplastic anemia associated with pregnancy (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Hemoglobin SS disease without crisis (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hemoglobin SS disease with crisis (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hemoglobin SS disease with vasoocclusive crisis (disorder) Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
IRIDA (Iron-refractory iron deficiency anemia) syndrome is a rare autosomal recessive iron metabolism disorder characterized by iron deficiency anemia (hypochromic, microcytic) that is often unresponsive to oral iron intake and partially responsive to parenteral iron treatment. Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Sickle cell anaemia in mother complicating childbirth Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Anemia due to pentose phosphate pathway defect Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
HNSHA due to pyrimidine-5'-nucleotidase deficiency Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
HNSHA due to phosphofructokinase deficiency Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hypoplastic anemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
HNSHA due to decreased adenosine deaminase activity Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Congenital atransferrinemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Anemia due to enzyme deficiency Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Congenital transferrin deficiency Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Acquired haemolytic anaemia associated with AIDS Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Anemia following acute postoperative blood loss (disorder) Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 1
Drug-induced immune hemolytic anemia, immune complex type Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Hapten type low affinity hemolytic anemia Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Microcytic hypochromic anemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hapten type high affinity hemolytic anemia Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Drug-induced immune hemolytic anemia Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Drug-induced immune hemolytic anemia, hapten type Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Drug-induced autoimmune hemolytic anemia Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Hypochromic microcytic anemia with iron overload (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Megaloblastic anemia due to folate deficiency due to increased requirement (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 4
Megaloblastic anemia due to folate deficiency in pregnancy and lactation (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 4
Megaloblastic anemia due to folate deficiency in prematurity (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 4
Acquired thiamine deficiency anemia (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Pancytopenia due to antineoplastic chemotherapy (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 6
Evans syndrome Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 3
Overhydrated hereditary stomatocytosis (OHSt) is a disorder of red cell membrane permeability to monovalent cations and is characterized clinically by hemolytic anemia. Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 5
Hemolytic disease of newborn co-occurrent and due to ABO immunization (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 8
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 10
Fanconi's anemia Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 4
Estren-Dameshek anemia Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 4
Southeast Asian ovalocytosis (SAO) is a rare hereditary red cell membrane defect characterized by the presence of oval-shaped erythrocytes and with most patients being asymptomatic or occasionally manifesting with mild symptoms such as pallor, jaundice, anemia and gallstones. Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 5
Mitochondrial myopathy and sideroblastic anemia belongs to the heterogeneous family of metabolic myopathies. It is characterized by progressive exercise intolerance manifesting in childhood, onset of sideroblastic anemia around adolescence, lactic acidemia, and mitochondrial myopathy. Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 6
STEAP3/TSAP6-related sideroblastic anemia is a very rare severe non-syndromic hypochromic anemia, which is characterized by transfusion-dependent hypochromic, poorly regenerative anemia, iron overload, resembling non-syndromic sideroblastic anemia except for increased erythrocyte protoporphyrin levels. Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Iron deficiency anemia due to blood loss (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 4
Acquired iron deficiency anemia due to decreased absorption (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 6
A rare genetic neurological disorder characterized by early-onset progressive leukoencephalopathy, severe developmental delay, early-onset or congenital deafness (only few cases reported without hearing loss), and visual impairment. All patients manifest calcifications in brain and spinal cord. Cognitive impairment, seizures, hypotonia, spastic tetraplegia or quadriplegia are observed in the majority of the patients. Variable features may include microcephaly and anemia. Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 6
Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease (disorder) Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 9
Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 9
Secondary autoimmune hemolytic anemia co-occurrent and due to rheumatic disorder (disorder) Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 9
Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis (disorder) Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 9
Secondary autoimmune haemolytic anaemia co-occurrent and due to systemic lupus erythematosus Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 10
A rare developmental defect during embryogenesis, a contiguous gene deletion syndrome, is a form of alpha-thalassemia characterized by microcytosis, hypochromia, normal hemoglobin (Hb) level or mild anemia, associated with developmental abnormalities. Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 8
Hereditary vitamin B12 deficiency anemia (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Hereditary folate deficiency anemia (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Anaemia due to metabolic disorder Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 3
Pericarditis associated with severe chronic anemia Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 2
Congenital hemolytic anemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
A constitutional microcytic, hypochromic anemia of varying severity that is clinically characterized by manifestations of anemia and iron overload and that may respond to treatment with pyridoxine and folic acid. Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 1
A form of constitutional sideroblastic anemia characterized by severe microcytic anemia, B-cell lymphopenia, panhypogammaglobulinemia and variable neurodegeneration. The disease presents in infancy with recurrent febrile illnesses, gastrointestinal disturbances, developmental delay, seizures, ataxia and sensorineural deafness. Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3

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