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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
Vitamin B12 deficiency anemia due to chronic atrophic gastritis (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Lymphocyte passenger syndrome following organ transplantation Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 3
Acute sequestration of spleen due to sickle cell thalassemia with crisis (disorder) Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 6
Acute splenic sequestration due to sickle cell hemoglobin C disease with crisis Interprets False Measurement of total haemoglobin concentration Inferred relationship Some 6
Vitamin B12 deficiency anemia following total gastrectomy (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Pernicious anaemia due to autoimmune disorder Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Mechanical hemolysis following insertion of prosthetic heart valve (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 4
Aase syndrome Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Thalassemia major Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Delta beta zero thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Beta plus thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Beta thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Alpha zero thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Alpha thalassemia (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hb Lepore thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Epsilon gamma delta beta^0^ thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Thalassemia-hemoglobin C disease Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Delta zero thalassemia (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Alpha plus thalassemia non deletion type (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
HPFH deletion type Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Alpha plus thalassaemia deletion type Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Beta zero thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
HPFH linked to beta-globulin gene cluster Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
^A^gamma delta beta^0^ thalassemia (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hereditary persistence of fetal hemoglobin, nondeletion type (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Thalassemia syndrome Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Epsilon gamma delta beta thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Alpha plus thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Sickle cell-thalassemia disease Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
HPFH A gamma beta^+^ thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
HPFH unlinked to beta-globulin gene cluster Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Homozygous beta thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Beta zero thalassemia deletion type Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Thalassemia with other hemoglobinopathy Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Beta plus thalassemia normal hemoglobin A>2< type 1 silent (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hemoglobin H disease Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
beta^+^ Thalassemia, normal Hb A>2<, type 2 Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Delta beta thalassemia (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Delta thalassaemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hereditary persistence of fetal hemoglobin thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Heterozygous thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
A>gamma< beta^+^ HPFH AND beta^0^ thalassaemia in cis Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Thalassemia intermedia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Beta zero thalassemia non deletion type (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Sickle cell-hemoglobin SS disease Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 1
Sickle cell trait with coexistent alpha-thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Alpha trait thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Beta thalassaemia intermedia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Homozygous alpha thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Alpha thalassemia-2 trait Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Haemoglobin Constant Spring trait Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hemoglobin Lepore trait Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Delta-beta-Lepore thalassaemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Alpha-beta thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Gamma thalassaemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Sickle cell anemia with high hemoglobin F Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Beta thalassaemia trait Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Acquired haemoglobin H disease Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hemoglobin SS disease with vasoocclusive crisis (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 1
A rare X-linked syndromic intellectual disability characterized by profound developmental delay, facial dysmorphism, genital abnormalities and alpha thalassemia. Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Dominant beta-thalassemia is a form of beta-thalassemia resulting in moderate to severe anemia. Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hemoglobin H constant spring thalassemia (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Haemoglobin Paksé disease Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 1
Hemoglobin Seal Rock disease (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 1
Acute sequestration of spleen due to sickle cell thalassemia with crisis (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 4
Acute splenic sequestration due to sickle cell hemoglobin C disease with crisis Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 4
Vitamin B12 deficiency anemia following gastrectomy (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hemoglobin finding Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 1
Hemoglobin E/beta thalassemia disease Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Upshaw-Schulman syndrome (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 4
Hematopoietic subsyndrome of acute radiation syndrome (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 5
A rare genetic hemolytic uremic syndrome (HUS) characterized by infantile onset of relapsing episodes of microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. The episodes are often preceded by viral infections. Affected individuals typically present persistent hypertension, hematuria, and proteinuria (sometimes in the nephrotic range) and develop chronic kidney disease with age. Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
A rare type of hemolytic uremic syndrome (HUS) characterized by the triad of hemolytic anemia due to generalized thrombotic microangiopathy, thrombocytopenia, and acute kidney injury, and most commonly occurring after acute gastroenteritis due to Shiga toxin-producing enterohemorrhagic Escherichia coli or Shigella dysenteriae. Other infectious causes of HUS include Streptococcus pneumoniae, HIV, Mycoplasma pneumoniae, Histoplasmosis, and Coxsackie virus. Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
A rare disorder characterized by hemolytic anemia, associated with metabolic acidosis and 5-oxoprolinuria in moderate forms, and with progressive neurological symptoms and recurrent bacterial infections in the most severe forms. Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Glutathione synthase deficiency without 5-oxoprolinuria Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Fanconi anemia of complementation group C Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Haemoglobin D beta plus thalassaemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Haemoglobin E beta plus thalassaemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Haemoglobin C beta plus thalassaemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hemoglobin E beta zero thalassemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hemoglobin D beta zero thalassemia (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Haemoglobin C beta zero thalassaemia Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Pancytopenia caused by colchicine (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Pancytopenia caused by non-steroidal anti-inflammatory agent (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Delta beta thalassemia trait (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Postpartum iron deficiency anemia (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Iron deficiency anemia during maternal intrapartum period (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Glutathione synthase deficiency with 5-oxoprolinuria Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Atypical haemolytic uraemic syndrome with complement gene abnormality Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 5
Atypical haemolytic uraemic syndrome with anti-factor H antibodies Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 5
A rare constitutional aplastic anaemia characterised by aplastic anaemia, intellectual disability, short stature, and microcephaly. Skin pigmentation or cafe au lait spots are often present. Majority of the patients present global developmental delay with impaired motor skills, learning disabilities, speech delay whereas some patients also may have behavioural problems including autistic features. Patients often develop premalignant myelodysplastic syndromes or leukaemia. Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 7
Pancytopenia caused by antidiabetic drug (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
A rare unclassified autoinflammatory syndrome characterised by neonatal onset pancytopenia, type I interferon-dependent multisystemic autoinflammation, painful rash with variable frequencies and haemophagocytic lymphohistiocytosis. Failure to thrive, fever, gastrointestinal/upper respiratory tract infections, enterocolitis, hepatosplenomegaly, myelofibrosis and neurodevelopmental delay are other common clinical features. Facial dysmorphism including macrocephaly, mild frontal bossing, sparse hair, mild hypertelorism, depressed nasal bridge can be present. Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 4
Beta thalassemia major in mother complicating pregnancy Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Beta thalassemia trait in mother complicating pregnancy (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3
Alpha thalassemia trait in mother complicating pregnancy (disorder) Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 2
Hereditary pyropoikilocytosis Interprets True Measurement of total haemoglobin concentration Inferred relationship Some 3

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