62574001: Erythropenia (finding)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
érythropénie	Is a	Cytopenia	false	Inferred relationship	Some
érythropénie	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
érythropénie	Is a	Red blood cell count - finding	false	Inferred relationship	Some
érythropénie	Finding site	Erythrocyte (cell)	false	Inferred relationship	Some
érythropénie	Interprets	Laboratory test	false	Inferred relationship	Some
érythropénie	Finding method (attribute)	Procedure	false	Inferred relationship	Some
érythropénie	Is a	Red blood cell count below reference range	false	Inferred relationship	Some
érythropénie	Interprets	Red blood cell count	false	Inferred relationship	Some	1
érythropénie	Has interpretation	Below reference range	false	Inferred relationship	Some	1
érythropénie	Has interpretation	Below reference range	false	Inferred relationship	Some	1
érythropénie	Interprets	Red blood cell count	false	Inferred relationship	Some	1
érythropénie	Interprets	Hematology procedure	false	Inferred relationship	Some	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Anémie post-chimiothérapie	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Oroya fever	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Acquired thrombotic thrombocytopenic purpura (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Autoimmune thrombotic thrombocytopenic purpura (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Drug induced thrombotic thrombocytopenic purpura (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Hemoglobin SS disease with vasoocclusive crisis (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Acute sickle cell splenic sequestration crisis (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Congenital hemolytic uremic syndrome (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Hemoglobin H constant spring thalassemia (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Anemia, pre-end stage renal disease on erythropoietin protocol	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Fetal anemia	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Anemia in mother complicating childbirth	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Sickle cell anaemia in mother complicating childbirth	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Iron deficiency anemia in mother complicating childbirth	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Thalassemia in mother complicating childbirth	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Thalassemia in mother complicating pregnancy	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Anemia in malignant neoplastic disease (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Chronic hemolytic anemia (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Anaemia in chronic kidney disease	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Anemia in end stage renal disease	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Hypochromic microcytic anemia with iron overload (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Anemia following acute postoperative blood loss (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Anaemia co-occurrent and due to chronic kidney disease stage 3	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Anaemia co-occurrent with human immunodeficiency virus infection	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
GATA binding protein 1 related thrombocytopenia with dyserythropoiesis (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Anaemia caused by zidovudine	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Aplastic anaemia co-occurrent with human immunodeficiency virus infection	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
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.	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
A rare X-linked syndromic intellectual disability characterized by profound developmental delay, facial dysmorphism, genital abnormalities and alpha thalassemia.	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Dominant beta-thalassemia is a form of beta-thalassemia resulting in moderate to severe anemia.	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
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.	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
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.	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Congenital autosomal recessive sideroblastic anemia (ARSA) is a non-syndromic, microcytic/hypochromic sideroblastic anemia, present from early infancy and characterized by severe microcytic anemia, which is not pyridoxine responsive, and increased serum ferritin.	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Anemia co-occurrent and due to chronic kidney disease stage 4 (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some	2
Anemia co-occurrent and due to chronic kidney disease stage 5 (disorder)	Has definitional manifestation	False	érythropénie	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.	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
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.	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Congenital dyserythropoietic anemia type IV (CDA IV) is a newly discovered form of CDA characterized by ineffective erythropoiesis and hemolysis that leads to severe anemia at birth.	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
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.	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
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.	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Megaloblastic anemia due to folate deficiency due to increased requirement (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some	5
Megaloblastic anemia due to folate deficiency in pregnancy and lactation (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some	5
Megaloblastic anemia due to folate deficiency in prematurity (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some	5
Hemolytic disease of newborn co-occurrent and due to ABO immunization (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Thrombocytopenia with congenital dyserythropoietic anemia is a rare hematological disorder, seen almost exclusively in males, characterized by moderate to severe thrombocytopenia with hemorrhages with or without the presence of mild to severe anemia.	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis.	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both.	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Secondary autoimmune haemolytic anaemia co-occurrent and due to systemic lupus erythematosus	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Secondary autoimmune hemolytic anemia co-occurrent and due to rheumatic disorder (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Some
Megaloblastic anaemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness	Is a	False	érythropénie	Inferred relationship	Some
Pure red cell aplasia	Is a	False	érythropénie	Inferred relationship	Some
Anemia	Is a	False	érythropénie	Inferred relationship	Some

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Reference Sets

Concept inactivation indicator reference set

SAME AS association reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
103993014	Erythropenia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
103994015	Erythrocytopenia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
499328013	Oligocytosis of red blood cells	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
499329017	Oligocythemia of red blood cells	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
499330010	Oligocythaemia of red blood cells	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
801761011	Erythropenia (finding)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
283311000077116	érythropénie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module