404227002: Hemolysis (observable entity)

SNOMED CT Concept\Observable entity (observable entity)\Any function or property that is not mainly morphologic or structural, including both measurable and observable features and physiologic actions\...

\Cell destruction, function (observable entity)\Blood cell destruction, function (observable entity)\Erythrocyte destruction\Hemolysis (observable entity)

\Hematologic function\Blood cell destruction, function (observable entity)\Erythrocyte destruction\Hemolysis (observable entity)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2004. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2148056014 Hemolysis (observable entity) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2153874014 Haemolysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2154897016 Hemolysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

7473031000241116 hémolyse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hemolysis (observable entity)	Is a	Hematologic function	false	Inferred relationship	Some
Hemolysis (observable entity)	Is a	Erythrocyte destruction	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
G-6-PD class IV variant anemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
G-6-PD class I variant anemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
G-6-PD class III variant anemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
Anemia due to mechanical damage	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
G-6-PD class II variant anemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
Polyagglutinable erythrocyte syndrome	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
Anemia due to abnormality extrinsic to the red cell	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
Anemia due to pentose phosphate pathway defect	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
Drug-induced enzyme deficiency anemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
Traumatic cardiac haemolytic anaemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
Anemia due to enzyme deficiency	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
Intracorpuscular haemolytic anaemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
Hemolytic anemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
Hemolytic anemia due to hexokinase deficiency	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
Chronic hemolytic anemia (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
Hemolytic anemia due to red cell enolase deficiency (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
Anemia due to membrane defect	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
Upshaw-Schulman syndrome (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	6
Intravascular hemolysis following ectopic pregnancy	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
Intravascular hemolysis following molar pregnancy	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
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	Hemolysis (observable entity)	Inferred relationship	Some	4
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	Hemolysis (observable entity)	Inferred relationship	Some	5
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	Hemolysis (observable entity)	Inferred relationship	Some	4
Glutathione synthase deficiency without 5-oxoprolinuria	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Glutathione synthase deficiency with 5-oxoprolinuria	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Atypical haemolytic uraemic syndrome with complement gene abnormality	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	7
Atypical haemolytic uraemic syndrome with anti-factor H antibodies	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	7
Moderate amount of hemolyzed blood detected in urine by dipstick (finding)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
Large amount of haemolysed blood detected in urine by dipstick	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
Small amount of hemolyzed blood detected in urine by dipstick (finding)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
Trace of hemolyzed blood detected in urine (finding)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
Hereditary pyropoikilocytosis	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
Hereditary cryohydrocytosis with normal stomatin is a rare, hereditary, hemolytic anemia due to a red cell membrane anomaly characterized by fatigue, mild anemia and pseudohyperkalemia due to a potassium leak from the red blood cells. A hallmark of this condition is that red blood cells lyse on storage at 4 degrees centigrade.	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	5
Overhydrated hereditary stomatocytosis (OHSt) is a disorder of red cell membrane permeability to monovalent cations and is characterized clinically by hemolytic anemia.	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
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	Hemolysis (observable entity)	Inferred relationship	Some	1
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	Hemolysis (observable entity)	Inferred relationship	Some	5
A rare hemolytic anemia characterized by combination of neurologic features, such as psychomotor delay, seizures, variable movement disorders, and hemolytic anemia with stomatocytosis, resulting in cation-leaky erythrocytes, pseudohyperkalemia, hemolytic crises and hepatosplenomegaly. Cataracts are also a presenting feature.	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	8

Start Previous Page 3 of 3

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
2148056014	Hemolysis (observable entity)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2153874014	Haemolysis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2154897016	Hemolysis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
7473031000241116	hémolyse	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module