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404227002: 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

0 descendants.

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 caused by complement Interprets True Hemolysis (observable entity) Inferred relationship Some 3
A rare, genetic, hematologic and neurologic disease characterized by chronic, Coombs-negative hemolysis associated with early-onset, relapsing, immune-mediated, inflammatory, axonal or demyelinating, sensory-motor, peripheral polyneuropathy and isolated or recurrent cerebrovascular events (in anterior or posterior circulation). 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 caused by 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
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 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
Hemolytic anemia 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 hemolytic anemia 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
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. Interprets True Hemolysis (observable entity) Inferred relationship Some 5
Autoimmune haemolytic anaemia caused by IgA plus complement Interprets True Hemolysis (observable entity) Inferred relationship Some 4
Traumatic cardiac haemolytic anaemia Interprets False Hemolysis (observable entity) Inferred relationship Some 3
Oroya fever Interprets True Hemolysis (observable entity) Inferred relationship Some 2
Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase 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 Interprets False 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 haemolytic anaemia Interprets True Hemolysis (observable entity) Inferred relationship Some 3
HNSHA due to glutathione reductase deficiency 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 is a rare hemolytic anemia due to an erythrocyte nucleotide metabolism disorder characterized by moderate to severe chronic nonspherocytic hemolytic anemia that may require regular blood transfusions and/or splenectomy and may be associated with psychomotor impairment. Interprets True Hemolysis (observable entity) Inferred relationship Some 3
March hemoglobinuria (disorder) Interprets True Hemolysis (observable entity) Inferred relationship Some 1
A rare, secondary, neonatal autoimmune disease characterized by onset of hemolytic anemia in the neonatal period associated with a positive direct antiglobulin test. Hepatosplenomegaly may be associated. 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
Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Interprets False Hemolysis (observable entity) Inferred relationship Some 3
Anemia 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 isoimmunization 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
A rare constitutional hemolytic anemia that is characterized by the association of Alport syndrome, midface hypoplasia, intellectual deficit and elliptocytosis. It has been described in two families. The syndrome is transmitted as an X-linked trait is caused by a contiguous gene deletion in Xq22.3 involving several genes including COL4A5, FACL4 and AMMECR1. 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 (disorder) Interprets True Hemolysis (observable entity) Inferred relationship Some 11
Posttransfusion purpura Interprets True Hemolysis (observable entity) Inferred relationship Some 5
purpura thrombopénique idiopathique 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
purpura thrombopénique congénital Interprets False Hemolysis (observable entity) Inferred relationship Some 6
Thrombocytopenic purpura associated with metabolic disorder (disorder) Interprets True Hemolysis (observable entity) Inferred relationship Some 6
purpura thrombopénique aigu idiopathique 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 hemolysis following insertion of prosthetic heart valve (disorder) 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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