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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
Familial pseudohyperkalemia (FP) is an inherited, mild, non-hemolytic subtype of hereditary stomatocytosis that is associated with a temperature-dependent anomaly in red cell membrane permeability to potassium that leads to high in vitro potassium levels in samples stored below 37°C. FP is not associated with additional hematological abnormalities, although affected individuals may show some mild abnormalities like macrocytosis. Interprets True Red blood cell count Inferred relationship Some 1
Megaloblastic anemia due to vitamin B12 deficiency secondary to intestinal disease (disorder) Interprets False Red blood cell count Inferred relationship Some 4
Vitamin B12 deficiency anaemia caused by drug Interprets False Red blood cell count Inferred relationship Some 5
Acquired iron deficiency anemia due to increased iron requirement (disorder) Interprets True Red blood cell count Inferred relationship Some 4
Beta-thalassemia - X-linked thrombocytopenia is a form of beta-thalassemia characterized by splenomegaly and petechiae, moderate thrombocytopenia, prolonged bleeding time due to platelet dysfunction, reticulocytosis and mild beta-thalassemia. Interprets False Red blood cell count Inferred relationship Some 1
Thalassemia in mother complicating pregnancy Interprets True Red blood cell count Inferred relationship Some 2
Anemia in mother complicating childbirth Interprets False Red blood cell count Inferred relationship Some 2
Thalassemia in mother complicating childbirth Interprets True Red blood cell count Inferred relationship Some 2
Iron deficiency anemia in mother complicating childbirth Interprets False Red blood cell count Inferred relationship Some 2
Traumatic cardiac haemolytic anaemia Interprets False Red blood cell count Inferred relationship Some 2
Stomatocytosis Interprets False Red blood cell count Inferred relationship Some 1
Acquired hemolytic anemia Interprets False Red blood cell count Inferred relationship Some 2
Hemolytic anemia due to nonlymphoid neoplasm Interprets True Red blood cell count Inferred relationship Some 2
A rare genetic haematologic disease characterised by mild chronic haemolytic anaemia (due to highly elevated adenosine deaminase activity in red blood cells resulting in their premature destruction), elevated reticulocyte count, splenomegaly and mild hyperbilirubinaemia. Other cells and tissues are not affected. Interprets True Red blood cell count Inferred relationship Some 2
Coombs negative hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 2
Haemolytic anaemia caused by Clostridium welchii Interprets True Red blood cell count Inferred relationship Some 4
Anemia due to mechanical damage Interprets False Red blood cell count Inferred relationship Some 2
Sickle cell-thalassemia disease Interprets False Red blood cell count Inferred relationship Some 3
Hereditary haemolytic anaemia Interprets True Red blood cell count Inferred relationship Some 2
Anemia due to abnormality extrinsic to the red cell Interprets False Red blood cell count Inferred relationship Some 2
Anemia of chronic renal failure Interprets False Red blood cell count Inferred relationship Some 1
Hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 2
Acute megaloblastic anemia caused by nitrous oxide (disorder) Interprets False Red blood cell count Inferred relationship Some 2
Coombs positive hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 2
Evans syndrome Interprets False Red blood cell count Inferred relationship Some 2
Hemolytic anemia caused by Bartonella Interprets True Red blood cell count Inferred relationship Some 2
Hemolytic uremic syndrome, adult type Interprets True Red blood cell count Inferred relationship Some 2
sindrome mielodisplastica: anemia refrattaria, senza sideroblasti ad anello, senza eccesso di blasti Interprets False Red blood cell count Inferred relationship Some 2
Myelodysplastic syndrome with ring sideroblasts and single lineage dysplasia (disorder) Interprets False Red blood cell count Inferred relationship Some 2
anémie réfractaire avec excès de blastes en transformation (clinique) Interprets False Red blood cell count Inferred relationship Some 2
Hemolytic uremic syndrome Interprets True Red blood cell count Inferred relationship Some 2
Acquired stomatocytosis Interprets False Red blood cell count Inferred relationship Some 1
Sickle cell-beta-thalassemia Interprets False Red blood cell count Inferred relationship Some 3
Sickle cell beta plus thalassaemia Interprets False Red blood cell count Inferred relationship Some 3
Sickle cell-beta^0^-thalassemia Interprets False Red blood cell count Inferred relationship Some 3
Sickle cell-delta beta^0^-thalassemia Interprets False Red blood cell count Inferred relationship Some 3
Refractory anemia without sideroblasts, so stated Interprets False Red blood cell count Inferred relationship Some 2
Hemolytic anemia due to glutathione metabolism disorder Interprets True Red blood cell count Inferred relationship Some 2
Non-autoimmune hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 2
Mechanical haemolytic anaemia Interprets False Red blood cell count Inferred relationship Some 2
Toxic hemolytic anemia Interprets False Red blood cell count Inferred relationship Some 2
Haemoglobinuria due to haemolysis from external causes Interprets True Red blood cell count Inferred relationship Some 2
Acquired spherocytosis Interprets True Red blood cell count Inferred relationship Some 2
Infantile pyknocytosis (disorder) Interprets True Red blood cell count Inferred relationship Some 2
Aplastic anemia due to radiation Interprets True Red blood cell count Inferred relationship Some 2
Anaemia of renal disease Interprets False Red blood cell count Inferred relationship Some 2
Megaloblastic anaemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Interprets True Red blood cell count Inferred relationship Some 2
Anaemia due to isoimmunisation Interprets False Red blood cell count Inferred relationship Some 2
Hereditary nonspherocytic haemolytic anaemia Interprets True Red blood cell count Inferred relationship Some 2
Anaemia secondary to renal failure Interprets False Red blood cell count Inferred relationship Some 2
Intracorpuscular haemolytic anaemia Interprets True Red blood cell count Inferred relationship Some 2
Diarrhea-negative hemolytic uremic syndrome (disorder) Interprets True Red blood cell count Inferred relationship Some 2
A rare disorder characterised by increased bone density (predominantly diaphyseal) and aregenerative corticosteroid-sensitive anaemia. The exact prevalence is unknown. Associated with mutations in the TBXAS1 gene (which encodes thromboxane synthase). Transmitted as an autosomal recessive trait. Interprets True Red blood cell count Inferred relationship Some 3
Myelodysplastic syndrome with excess blasts (disorder) Interprets False Red blood cell count Inferred relationship Some 2
Sickle cell-thalassemia disease with crisis (disorder) Interprets False Red blood cell count Inferred relationship Some 3
Sickle cell-thalassemia disease without crisis (disorder) Interprets False Red blood cell count Inferred relationship Some 3
A rare genetic disease characterized by lethal non-spherocytic, non-immune hemolytic anemia, in association with abnormalities of the external genitalia (such as micropenis and hypospadias). Reported dysmorphic features include flat occiput, dimpled earlobes, deep plantar creases, and increased space between the first and second toes. There have been no further descriptions in the literature since 1995. Interprets True Red blood cell count Inferred relationship Some 8
A rare genetic disease characterized by cystic fibrosis, gastritis associated with Helicobacter pylori, folate deficiency megaloblastic anemia, and intellectual disability. There have been no further descriptions in the literature since 1991. Interprets False Red blood cell count Inferred relationship Some 6
A very rare non-syndromic autosomal recessive pyridoxine-refractory sideroblastic anemia due to a splice defect of glutaredoxin-5 (GLRX5) described in a single patient with adult onset microcytic hypochromic anemia with liver iron overload and type 2 diabetes. Interprets False Red blood cell count Inferred relationship Some 6
Anemia, pre-end stage renal disease on erythropoietin protocol Interprets False Red blood cell count Inferred relationship Some 1
Autoimmune hemolytic anemia caused by immunoglobulin G (disorder) Interprets False Red blood cell count Inferred relationship Some 1
Anemia due to radiation Interprets False Red blood cell count Inferred relationship Some 1
Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Interprets True Red blood cell count Inferred relationship Some 2
Autoimmune hemolytic anemia caused by complement Interprets False Red blood cell count Inferred relationship Some 1
Thiamine-responsive megaloblastic anemia Interprets True Red blood cell count Inferred relationship Some 1
Goats' milk anemia Interprets False Red blood cell count Inferred relationship Some 1
Anemia caused by insect venom (disorder) Interprets False Red blood cell count Inferred relationship Some 1
Anemia of thyroid dysfunction Interprets False Red blood cell count Inferred relationship Some 1
Anemia of gonadal dysfunction Interprets False Red blood cell count Inferred relationship Some 1
G-6-PD class I variant anemia Interprets False Red blood cell count Inferred relationship Some 1
G-6-PD class III variant anemia Interprets False Red blood cell count Inferred relationship Some 1
Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Interprets True Red blood cell count Inferred relationship Some 2
Hereditary spherocytosis due to spectrin deficiency Interprets True Red blood cell count Inferred relationship Some 2
Acute megaloblastic anaemia due to dialysis Interprets True Red blood cell count Inferred relationship Some 1
Anaemia caused by oxygen Interprets False Red blood cell count Inferred relationship Some 1
Anemia of adrenal dysfunction Interprets False Red blood cell count Inferred relationship Some 1
Mild hereditary spherocytosis due to spectrin deficiency Interprets True Red blood cell count Inferred relationship Some 2
Autoimmune haemolytic anaemia caused by IgA plus complement Interprets False Red blood cell count Inferred relationship Some 1
Hereditary spherocytosis due to deficiency of protein 4.2 Interprets True Red blood cell count Inferred relationship Some 2
G-6-PD class II variant anemia Interprets False Red blood cell count Inferred relationship Some 1
Megaloblastic anemia due to inborn errors of metabolism Interprets True Red blood cell count Inferred relationship Some 1
Megaloblastic anemia due to error of folate metabolism Interprets True Red blood cell count Inferred relationship Some 1
Hemolytic anemia due to infection Interprets True Red blood cell count Inferred relationship Some 2
Anemia caused by copper Interprets False Red blood cell count Inferred relationship Some 1
HNSHA due to hexokinase deficiency Interprets True Red blood cell count Inferred relationship Some 1
Anemia caused by heat (disorder) Interprets True Red blood cell count Inferred relationship Some 1
Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Interprets True Red blood cell count Inferred relationship Some 2
Juvenile type megaloblastic anemia Interprets True Red blood cell count Inferred relationship Some 1
Anaemia of pituitary deficiency Interprets False Red blood cell count Inferred relationship Some 1
Megaloblastic anemia due to congenital deficiency of intrinsic factor Interprets True Red blood cell count Inferred relationship Some 1
Hemolytic anemia with emphysema AND cutis laxa Interprets False Red blood cell count Inferred relationship Some 1
Glucose-6-phosphate dehydrogenase deficiency anemia Interprets True Red blood cell count Inferred relationship Some 1
Autoimmune hemolytic anemia caused by immunoglobulin G plus complement (disorder) Interprets False Red blood cell count Inferred relationship Some 1
Megaloblastic anemia due to error of cobalamin metabolism Interprets True Red blood cell count Inferred relationship Some 1
Anemia of parathyroid dysfunction Interprets False Red blood cell count Inferred relationship Some 1
Hereditary spherocytosis due to beta spectrin defect Interprets True Red blood cell count Inferred relationship Some 2
Autoimmune hemolytic anemia caused by immunoglobulin M Interprets False Red blood cell count Inferred relationship Some 1
Acute megaloblastic anemia secondary to total parenteral nutrition Interprets False Red blood cell count Inferred relationship Some 1
Anemia caused by arsenic hydride Interprets False Red blood cell count Inferred relationship Some 1
Severe hereditary spherocytosis due to spectrin deficiency Interprets True Red blood cell count Inferred relationship Some 2
G-6-PD class V variant anemia Interprets False Red blood cell count Inferred relationship Some 1

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