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14089001: Red blood cell count (procedure)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
23984019 Red blood cell count en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
23985018 RBC count en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
476071015 RBC - Red blood cell count en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
739997012 Red blood cell count (procedure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

13 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Red blood cell count Is a Blood cell count true Inferred relationship Some
Red blood cell count Is a Red blood cell test false Inferred relationship Some
Red blood cell count Method Investigation - action false Inferred relationship Some
Red blood cell count Has measured component (attribute) Erythrocyte (cell) false Inferred relationship Some
Red blood cell count Has intent Diagnostic intent (qualifier value) false Inferred relationship Some
Red blood cell count Component Hematology observable false Inferred relationship Some
Red blood cell count Component Erythrocyte (cell) true Inferred relationship Some 1
Red blood cell count Has specimen Red blood cell fluid specimen (specimen) false Inferred relationship Some
Red blood cell count Method Evaluation - action false Inferred relationship Some
Red blood cell count Method Measurement - action false Inferred relationship Some 2
Red blood cell count Method Measurement - action true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder Interprets True Red blood cell count Inferred relationship Some 4
Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis (disorder) Interprets True Red blood cell count Inferred relationship Some 4
Secondary autoimmune hemolytic anemia co-occurrent and due to rheumatic disorder (disorder) Interprets True Red blood cell count Inferred relationship Some 4
Lymphocyte passenger syndrome following organ transplantation Interprets True Red blood cell count Inferred relationship Some 5
G-6-PD variant enzyme deficiency anemia Interprets True Red blood cell count Inferred relationship Some 2
G-6-PD class V variant anemia Interprets True Red blood cell count Inferred relationship Some 2
G-6-PD class IV variant anemia Interprets True Red blood cell count Inferred relationship Some 2
G-6-PD class I variant anemia Interprets True Red blood cell count Inferred relationship Some 2
G-6-PD class III variant anemia Interprets True Red blood cell count Inferred relationship Some 2
Anemia due to mechanical damage Interprets True Red blood cell count Inferred relationship Some 1
G-6-PD class II variant anemia Interprets True Red blood cell count Inferred relationship Some 2
Anemia due to pentose phosphate pathway defect Interprets True Red blood cell count Inferred relationship Some 2
Drug-induced enzyme deficiency anemia Interprets True Red blood cell count Inferred relationship Some 3
Traumatic cardiac haemolytic anaemia Interprets True Red blood cell count Inferred relationship Some 1
Traumatic hemolytic anemia (disorder) Interprets True Red blood cell count Inferred relationship Some 2
Hemolytic anemia due to red cell enolase deficiency (disorder) Interprets True Red blood cell count Inferred relationship Some 3
Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency Interprets True Red blood cell count Inferred relationship Some 3
Antibody-mediated anemia Interprets True Red blood cell count Inferred relationship Some 2
Polyagglutinable erythrocyte syndrome Interprets True Red blood cell count Inferred relationship Some 2
Anemia due to abnormality extrinsic to the red cell Interprets True Red blood cell count Inferred relationship Some 1
Vitamin B12 deficiency anemia following gastrectomy (disorder) Interprets True Red blood cell count 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 Red blood cell count Inferred relationship Some 1
Epsilon gamma delta beta^0^ thalassemia Interprets True Red blood cell count Inferred relationship Some 1
Alpha plus thalassemia non deletion type (disorder) Interprets True Red blood cell count Inferred relationship Some 1
Alpha plus thalassaemia deletion type Interprets True Red blood cell count Inferred relationship Some 1
A rare, endocrine disease characterized by early onset of polycythemia, and later occurring multiple paraganglioma. Clinical presentation includes hypertension, headaches, fatigue, nausea, anxiety, and high concentration of red blood cells, leading to increased risk of stroke and pulmonary thromboembolism. Interprets True Red blood cell count Inferred relationship Some 1
Upshaw-Schulman syndrome (disorder) Interprets True Red blood cell count Inferred relationship Some 3
Hematopoietic subsyndrome of acute radiation syndrome (disorder) Interprets True Red blood cell count Inferred relationship Some 4
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 Red blood cell count Inferred relationship Some 9
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 Red blood cell count Inferred relationship Some 2
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 Red blood cell count Inferred relationship Some 2
Glutathione synthase deficiency without 5-oxoprolinuria Interprets True Red blood cell count Inferred relationship Some 2
Fanconi anemia of complementation group C Interprets True Red blood cell count Inferred relationship Some 2
Pancytopenia caused by colchicine (disorder) Interprets True Red blood cell count Inferred relationship Some 2
Pancytopenia caused by non-steroidal anti-inflammatory agent (disorder) Interprets True Red blood cell count Inferred relationship Some 2
Postpartum iron deficiency anemia (disorder) Interprets True Red blood cell count Inferred relationship Some 1
Iron deficiency anemia during maternal intrapartum period (disorder) Interprets True Red blood cell count Inferred relationship Some 1
Glutathione synthase deficiency with 5-oxoprolinuria Interprets True Red blood cell count Inferred relationship Some 2
Atypical haemolytic uraemic syndrome with complement gene abnormality Interprets True Red blood cell count Inferred relationship Some 4
Atypical haemolytic uraemic syndrome with anti-factor H antibodies Interprets True Red blood cell count Inferred relationship Some 4
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 Red blood cell count Inferred relationship Some 5
Pancytopenia caused by antidiabetic drug (disorder) Interprets True Red blood cell count Inferred relationship Some 1
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 Red blood cell count Inferred relationship Some 3
Hereditary pyropoikilocytosis Interprets True Red blood cell count Inferred relationship Some 1
Dehydrated hereditary stomatocytosis (DHS) is a rare hemolytic anemia characterized by a decreased red cell osmotic fragility due to a defect in cation permeability, resulting in red cell dehydration and mild to moderate compensated hemolysis. Pseudohyperkalemia (loss of potassium ions from red cells on storage at room temperature) is sometimes observed. Interprets True Red blood cell count Inferred relationship Some 2
Early-onset neurodegeneration, choreoathetoid movement, microcytic anemia due to iron responsive element binding protein 2 gene mutation (disorder) Interprets True Red blood cell count Inferred relationship Some 3

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