404227002: Hemolysis (observable entity)

SNOMED CT Concept\Observable entity\Function (observable entity)\...

\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:

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
Hemolytic disease of fetus OR newborn due to RhD isoimmunization (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Autoimmune hemolytic anemia due to complement	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Primary CD59 deficiency	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Drug-induced immune hemolytic anemia, immune complex type	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Hemolytic anemia due to Bartonella	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	5
Anaemia due to isoimmunisation	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Secondary autoimmune haemolytic anaemia co-occurrent and due to systemic lupus erythematosus	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Idiopathic chronic cold agglutinin disease	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
HNSHA due to phosphofructokinase deficiency	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Duffy isoimmunisation of the newborn	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
G-6-PD variant enzyme deficiency anemia	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	3
HNSHA due to triosephosphate isomerase deficiency	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Kidd isoimmunization of the newborn	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
G-6-PD class V variant anemia	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	3
Failed attempted abortion with intravascular hemolysis (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
Hemolytic anemia due to hexokinase deficiency	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	3
Hapten type low affinity hemolytic anemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Anemia due to mechanical damage	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	3
Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Hemolytic anemia due to glutathione metabolism disorder	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Miscarriage with intravascular hemolysis (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Warm autoimmune hemolytic anemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Lethal hemolytic anemia and genital anomaly syndrome (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Diarrhea-negative hemolytic uremic syndrome (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	6
Secondary autoimmune hemolytic anemia co-occurrent and due to rheumatic disorder (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Evans syndrome	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	5
Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Hemolytic anemia due to babesiosis	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Chronic hemolytic anemia (disorder)	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	3
Haemolytic anaemia due to nonlymphoid neoplasm	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
G-6-PD class III variant anemia	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	3
Secondary warm-type haemolytic anaemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Hereditary nonspherocytic haemolytic anaemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Maternal autoimmune hemolytic anemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
HNSHA due to gamma glutamyl cysteine synthetase deficiency	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Familial haemolytic uraemic syndrome	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	5
Autoimmune hemolytic anemia due to IgA plus complement	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Traumatic cardiac hemolytic anemia	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	3
Oroya fever	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
hemolytisk anemi orsakad av pyruvatkinasbrist	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	3
Hemolytic anemia due to triose phosphate isomerase deficiency	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Illegal abortion with intravascular hemolysis (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Anemia due to enzyme deficiency	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	3
HNSHA due to glucose phosphate isomerase deficiency	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Immediate hemolytic transfusion reaction	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
Hereditary hemolytic anemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
HNSHA due to pyrimidine-5'-nucleotidase deficiency	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Hemolytic disorder	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
Hemolytic anemia due to adenylate kinase deficiency (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
March hemoglobinuria (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
Neonatal autoimmune haemolytic anaemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Post-viral paroxysmal cold hemoglobinuria	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
G-6-PD class II variant anemia	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	3
ärftlig icke-sfärocytär hemolytisk anemi orsakad av aldolas A-brist	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	3
Anaemia due to abnormality extrinsic to the red cell	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	3
Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
HNSHA due to glutathione synthetase deficiency	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Rhesus isoimmunisation due to anti-E	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Induced termination of pregnancy complicated by intravascular haemolysis	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
Secondary paroxysmal cold hemoglobinuria	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Hemolytic anemia	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	3
Atypical isoimmunization of newborn	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Hereditary elliptocytosis due to glycophorin C deficiency	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Hereditary elliptocytosis with transient poikilocytosis	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
Hereditary elliptocytosis	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Hereditary elliptocytosis due to deficiency of protein 4.1	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Hereditary elliptocytosis due to abnormal protein 4.1	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Hereditary elliptocytosis due to beta spectrin defect in self-association	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	6
Hereditary elliptocytosis due to alpha spectrin defect	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Atypical haemolytic uraemic syndrome	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	6
Primaquine sensitivity anaemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Post-artesunate delayed haemolysis	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Hemolytic disease of fetus due to ABO immunization	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Thrombocytopenic purpura	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	2
Chronic idiopathic thrombocytopenic purpura	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	11
Posttransfusion purpura	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	5
idiopatisk trombocytopen purpura	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	11
Post infectious thrombocytopenic purpura	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	9
Thrombocytopenic purpura due to defective platelet production (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	5
Thrombocytopenic purpura due to platelet consumption (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	5
Congenital thrombocytopenic purpura	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	6
Thrombocytopenic purpura associated with metabolic disorder (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	6
akut idiopatisk trombocytopen purpura	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	10
Haemolytic anaemia of pregnancy	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Hemolytic anemia due to red cell enolase deficiency (disorder)	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	4
Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency	Interprets	False	Hemolysis (observable entity)	Inferred relationship	Some	4
Drug-induced non autoimmune haemolytic anaemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Homozygous hereditary elliptocytosis (disorder)	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	4
Lymphocyte passenger syndrome following organ transplantation	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	6
Mechanical haemolysis due to prosthetic valve	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	3
Coombs negative hemolytic anemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
Coombs positive hemolytic anemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
G-6-PD variant enzyme deficiency anemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
G-6-PD class V variant anemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1
G-6-PD class IV variant anemia	Interprets	True	Hemolysis (observable entity)	Inferred relationship	Some	1

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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
1572001000052114	hemolys	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)