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	Existential restriction modifier (core metadata concept)
érythropénie	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
érythropénie	Is a	Red blood cell count - finding	false	Inferred relationship	Existential restriction modifier (core metadata concept)
érythropénie	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)
érythropénie	Interprets	Laboratory test	false	Inferred relationship	Existential restriction modifier (core metadata concept)
érythropénie	Finding method	Procedure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
érythropénie	Is a	Red blood cell count below reference range	false	Inferred relationship	Existential restriction modifier (core metadata concept)
érythropénie	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
érythropénie	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
érythropénie	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
érythropénie	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
érythropénie	Interprets	Hematology procedure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Anémie post-chimiothérapie	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Oroya fever	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Acquired thrombotic thrombocytopenic purpura (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Autoimmune thrombotic thrombocytopenic purpura (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Drug induced thrombotic thrombocytopenic purpura (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Hemoglobin SS disease with vasoocclusive crisis (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Acute sickle cell splenic sequestration crisis (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hemolytic uremic syndrome (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Hemoglobin H constant spring thalassemia (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Anemia, pre-end stage renal disease on erythropoietin protocol	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Fetal anemia	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Anemia in mother complicating childbirth	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Sickle cell anemia in mother complicating childbirth	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Iron deficiency anemia in mother complicating childbirth	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassemia in mother complicating childbirth (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassemia in mother complicating pregnancy (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Anaemia in malignant neoplastic disease	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Chronic haemolytic anaemia	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Anaemia in chronic kidney disease	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Anemia in end stage renal disease	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypochromic microcytic anemia with iron overload (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Anemia following acute postoperative blood loss (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Anaemia co-occurrent and due to chronic kidney disease stage 3	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Anemia co-occurrent with human immunodeficiency virus infection (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
GATA binding protein 1 related thrombocytopenia with dyserythropoiesis (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Anemia caused by zidovudine (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Aplastic anaemia co-occurrent with human immunodeficiency virus infection	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Dehydrated hereditary stomatocytosis (DHS) is a rare haemolytic anaemia characterised by a decreased red cell osmotic fragility due to a defect in cation permeability, resulting in red cell dehydration and mild to moderate compensated haemolysis. Pseudohyperkalaemia (loss of potassium ions from red cells on storage at room temperature) is sometimes observed.	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha thalassemia X-linked intellectual disability syndrome (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Dominant beta-thalassemia (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
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	Existential restriction modifier (core metadata concept)
Beta thalassemia X-linked thrombocytopenia syndrome	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal recessive sideroblastic anemia (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Anemia co-occurrent and due to chronic kidney disease stage 4 (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Anemia co-occurrent and due to chronic kidney disease stage 5 (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autoimmune hemolytic anemia mixed type	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Lethal hemolytic anemia and genital anomaly syndrome (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital dyserythropoietic anemia type IV (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Adult-onset autosomal recessive sideroblastic anemia	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Cystic fibrosis with gastritis and megaloblastic anemia syndrome (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Megaloblastic anemia due to folate deficiency due to increased requirement (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Megaloblastic anaemia due to folate deficiency in pregnancy and lactation	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Megaloblastic anemia due to folate deficiency in prematurity (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Hemolytic disease of newborn co-occurrent and due to ABO immunization (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
X-linked congenital dyserythropoietic anemia with thrombocytopenia (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial haemolytic uraemic syndrome	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Secondary autoimmune hemolytic anemia co-occurrent and due to systemic lupus erythematosus (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Secondary autoimmune haemolytic anaemia co-occurrent and due to rheumatic disorder	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis (disorder)	Has definitional manifestation	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness (disorder)	Is a	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Pure red cell aplasia	Is a	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)
Anaemia	Is a	False	érythropénie	Inferred relationship	Existential restriction modifier (core metadata concept)

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Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

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
103993014	Erythropenia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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	Only initial character 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	Only initial character 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	Only initial character 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	Only initial character 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	Only initial character 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
283311000077116	érythropénie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module