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263654008: Abnormal (qualifier value)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
391916010 Abnormal en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
655800016 Abnormal (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
139711000077111 anormal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
2337331000195117 Abnorm de Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
2337341000195113 Auffällig de Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Abnormal Is a Normality findings true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
von Willebrand factor inhibitor disorder Has interpretation True Abnormal Inferred relationship Some 2
Factor VIII inhibitor disorder (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Congenital fibrinogen abnormality Has interpretation True Abnormal Inferred relationship Some 2
Parvoviral aplastic crisis Has interpretation True Abnormal Inferred relationship Some 7
A rare congenital disorder of glycosylation characterised by cerebral and portal vein thrombosis, portal hypertension, macrocephaly, and persistent absence seizures. Additional reported features include mild to moderate global developmental delay and intellectual disability, as well as thrombocytopenia. Brain imaging may show variable stages of infarction and cerebral and cerebellar atrophy. Has interpretation True Abnormal Inferred relationship Some 2
Acquired auditory processing disorder Has interpretation True Abnormal Inferred relationship Some 2
Humoral immunologic aplastic anemia Has interpretation True Abnormal Inferred relationship Some 8
purpura thrombopénique aigu idiopathique Has interpretation False Abnormal Inferred relationship Some 5
Dysphasia as late effect of cerebrovascular disease Has interpretation True Abnormal Inferred relationship Some 3
A rare hemorrhagic disorder caused by congenital deficiency of alpha2 antiplasmin, leading to dysregulated fibrinolysis and is characterized by a hemorrhagic tendency presenting from childhood with prolonged bleeding and ecchymoses following minor trauma and spontaneous bleeding episodes (often in unusual locations like diaphysis of long bones). Has interpretation True Abnormal Inferred relationship Some 2
Acquired fibrinogen abnormality Has interpretation True Abnormal Inferred relationship Some 2
Thrombocytopenic purpura Has interpretation True Abnormal Inferred relationship Some 4
Acquired thrombocytopenia Has interpretation True Abnormal Inferred relationship Some 3
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia is a rare, genetic, constitutional dyserythropoietic anemia disorder characterized by moderate to severe anemia without thrombocytopenia, variable degrees of neutropenia, and bone marrow biopsy findings of trilineage dysplasia and hypocellularity of erythroid and granulocytic lineages. Peripheral blood findings include anisocytosis, macrocytosis, poikilocytosis, elliptocytes, and fragmented erythrocytes. Has interpretation True Abnormal Inferred relationship Some 7
Factor I inhibitor disorder Has interpretation True Abnormal Inferred relationship Some 2
Acquired coagulation disorder Has interpretation True Abnormal Inferred relationship Some 2
Transient neonatal thrombocytopenia Has interpretation False Abnormal Inferred relationship Some 3
Purpura fulminans Has interpretation True Abnormal Inferred relationship Some 5
Acquired factor VII deficiency disease Has interpretation True Abnormal Inferred relationship Some 2
Secondary cryofibrinogenemia Has interpretation True Abnormal Inferred relationship Some 2
Hereditary isolated aplastic anemia is a rare, genetic, constitutional aplastic anemia disorder characterized by severe peripheral blood pancytopenia and bone marrow hypoplasia in multiple individuals of a family, in the absence of any somatic symptoms. Abnormal bleeding, as well as erythrocyte macrocytosis, is reported and patients usually become transfusion dependent. Has interpretation True Abnormal Inferred relationship Some 8
Inherited platelet disorder Has interpretation True Abnormal Inferred relationship Some 2
Speech and language deficit due to and following embolic cerebrovascular accident (disorder) Has interpretation False Abnormal Inferred relationship Some 3
Platelet type pseudo-von Willebrand disease Has interpretation False Abnormal Inferred relationship Some 3
Constitutional aplastic anemia Has interpretation False Abnormal Inferred relationship Some 7
Glycoprotein Ia defect Has interpretation True Abnormal Inferred relationship Some 2
Glycoprotein Ib defect Has interpretation True Abnormal Inferred relationship Some 2
Uremic thrombocytopenia (disorder) Has interpretation True Abnormal Inferred relationship Some 3
Acquired storage pool deficiency (platelets) Has interpretation False Abnormal Inferred relationship Some 3
Acquired factor XIII deficiency disease Has interpretation True Abnormal Inferred relationship Some 2
Thrombocytopenia due to massive blood transfusion Has interpretation True Abnormal Inferred relationship Some 3
Cyclooxygenase deficiency Has interpretation True Abnormal Inferred relationship Some 2
Infection-associated purpura Has interpretation True Abnormal Inferred relationship Some 3
Thromboxane synthetase deficiency Has interpretation True Abnormal Inferred relationship Some 2
Aplastic anemia with AIDS (acquired immunodeficiency syndrome) Has interpretation True Abnormal Inferred relationship Some 8
Acquired platelet disorder Has interpretation False Abnormal Inferred relationship Some 2
May-Hegglin anomaly Has interpretation False Abnormal Inferred relationship Some 3
Thrombocytopenia caused by alcohol (disorder) Has interpretation True Abnormal Inferred relationship Some 3
Thrombocytopenia due to sequestration Has interpretation True Abnormal Inferred relationship Some 3
Thrombophilia due to malignant neoplasm Has interpretation True Abnormal Inferred relationship Some 2
Congenital thrombocytopenia (disorder) Has interpretation False Abnormal Inferred relationship Some 3
Articulation disorder due to hyperkinesis (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Neonatal coagulation disorder Has interpretation True Abnormal Inferred relationship Some 2
Aplastic anemia caused by toxic cause Has interpretation True Abnormal Inferred relationship Some 8
Fanconi's anemia Has interpretation True Abnormal Inferred relationship Some 7
Spastic dysphonia Has interpretation True Abnormal Inferred relationship Some 2
Pancytopenia Has interpretation True Abnormal Inferred relationship Some 6
Acquired hypoplasminogenemia Has interpretation True Abnormal Inferred relationship Some 2
Drug-induced immune thrombocytopenia Has interpretation True Abnormal Inferred relationship Some 3
Aplastic anaemia Has interpretation True Abnormal Inferred relationship Some 7
Neonatal thrombocytopenia due to exchange transfusion Has interpretation True Abnormal Inferred relationship Some 3
Idiopathic aplastic anaemia Has interpretation True Abnormal Inferred relationship Some 7
Thrombocytopaenia co-occurrent and due to alcoholism Has interpretation True Abnormal Inferred relationship Some 4
An autoimmune coagulation disorder characterized by isolated thrombocytopenia (a platelet count <100,000/microL), in the absence of any underlying disorder that may be associated with thrombocytopenia. Has interpretation True Abnormal Inferred relationship Some 3
Bullous ichthyosiform erythroderma Has interpretation True Abnormal Inferred relationship Some 3
Platelet dysfunction associated with uremia (disorder) Has interpretation False Abnormal Inferred relationship Some 3
Dysphonia of Gilles de la Tourette's syndrome Has interpretation True Abnormal Inferred relationship Some 2
Speech and language deficit due to and following hemorrhagic cerebrovascular accident (disorder) Has interpretation False Abnormal Inferred relationship Some 3
Alloimmune thrombocytopenia Has interpretation True Abnormal Inferred relationship Some 3
Accidental coumarin overdose Has interpretation False Abnormal Inferred relationship Some 2
Catastrophic antiphospholipid syndrome (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Transient acquired pure red cell aplasia Has interpretation False Abnormal Inferred relationship Some 7
Coumarin overdose of undetermined intent Has interpretation False Abnormal Inferred relationship Some 2
Radiation thrombocytopenia Has interpretation True Abnormal Inferred relationship Some 3
Cryofibrinogenemia Has interpretation True Abnormal Inferred relationship Some 2
Platelet storage pool defect Has interpretation False Abnormal Inferred relationship Some 3
Accidental warfarin overdose Has interpretation False Abnormal Inferred relationship Some 2
Heparin-induced thrombocytopenia with thrombosis Has interpretation True Abnormal Inferred relationship Some 5
Acquired factor XII deficiency disease Has interpretation True Abnormal Inferred relationship Some 2
Familial alpha>2< adrenergic receptor defect in platelets Has interpretation False Abnormal Inferred relationship Some 2
Autoimmune thrombotic thrombocytopenic purpura (disorder) Has interpretation False Abnormal Inferred relationship Some 9
Voice disorder due to psychosexual conflict Has interpretation True Abnormal Inferred relationship Some 2
HELLP syndrome Has interpretation True Abnormal Inferred relationship Some 4
Primary cryofibrinogenemia Has interpretation True Abnormal Inferred relationship Some 2
Dysphonia of palatopharyngolaryngeal myoclonus Has interpretation True Abnormal Inferred relationship Some 5
Acquired thrombotic thrombocytopenic purpura (disorder) Has interpretation False Abnormal Inferred relationship Some 9
thrombophilie due aux anticorps antiphospholipides Has interpretation False Abnormal Inferred relationship Some 2
Fluency disorder due to and following cerebrovascular accident (disorder) Has interpretation True Abnormal Inferred relationship Some 3
Hereditary factor I deficiency disease Has interpretation True Abnormal Inferred relationship Some 2
Hemorrhagic disorder due to hyperheparinemia Has interpretation True Abnormal Inferred relationship Some 2
A rare, genetic, isolated, focal palmoplantar keratoderma disease characterized by focal thickening of the skin of the soles, and often of the palms, associated with minimal or no nail involvement. Patients frequently present non-epidermolytic painful plantar blistering and, occasionally, subtle oral leukokeratosis or plantar hyperhidrosis. Has interpretation True Abnormal Inferred relationship Some 2
A rare constitutional aplastic anemia disorder characterized by severe hypo/aplastic anemia or pancytopenia associated with skeletal anomalies (such as radial/ulnar defects and hand/digit abnormalities) and an increased risk of leukemia. There have been no further descriptions in the literature since 1995. Has interpretation False Abnormal Inferred relationship Some 7
Thrombophilia due to hormone therapy Has interpretation True Abnormal Inferred relationship Some 2
Evans syndrome Has interpretation True Abnormal Inferred relationship Some 7
Illegal abortion with defibrination syndrome Has interpretation False Abnormal Inferred relationship Some 2
Aplastic anemia associated with metabolic alteration (disorder) Has interpretation True Abnormal Inferred relationship Some 8
Acquired hypofibrinogenemia Has interpretation True Abnormal Inferred relationship Some 2
Heparin overdose Has interpretation False Abnormal Inferred relationship Some 2
A rare syndrome with combined immunodeficiency characterized by a variable clinical presentation ranging from asymptomatic individuals to potentially life-threatening, recurrent bacterial infections associated with progressive loss of serum immunoglobulins and B cells. Has interpretation False Abnormal Inferred relationship Some 6
Aplastic anemia associated with pancreatitis (disorder) Has interpretation True Abnormal Inferred relationship Some 8
Deficiency of coagulation factor due to liver disease Has interpretation True Abnormal Inferred relationship Some 3
Acquired coagulation factor deficiency Has interpretation True Abnormal Inferred relationship Some 2
Accidental heparin overdose Has interpretation False Abnormal Inferred relationship Some 2
Deficiency of coagulation factor due to vitamin K deficiency Has interpretation True Abnormal Inferred relationship Some 2
Intentional heparin overdose (disorder) Has interpretation False Abnormal Inferred relationship Some 2
Acquired language comprehension impairment (disorder) Has interpretation True Abnormal Inferred relationship Some 3
Pancytopenia caused by immunosuppressant Has interpretation True Abnormal Inferred relationship Some 7
Acquired factor II deficiency Has interpretation True Abnormal Inferred relationship Some 2
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder) Has interpretation False Abnormal Inferred relationship Some 7
surdose d'héparine d'intention indéterminée Has interpretation False Abnormal Inferred relationship Some 2
Coumarin overdose Has interpretation False Abnormal Inferred relationship Some 2

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