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263654008: Abnormal (qualifier value)

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

Descriptions:

Id Description Lang Type Status Case? Module
391916010 Abnormal en Synonym Active Entire term case insensitive SNOMED CT core module
655800016 Abnormal (qualifier value) en Fully specified name Active Entire term case insensitive SNOMED CT core module

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Abnormal Is a Normality findings true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary combined deficiency of vitamin K-dependent clotting factors Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Platelet dysfunction caused by aspirin Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Thrombocytopenia due to defective platelet production Has interpretation False Abnormal Inferred relationship Existential restriction modifier 3
Psychogenic voice disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Pancytopenia with pancreatitis Has interpretation True Abnormal Inferred relationship Existential restriction modifier 7
Speech and language deficit as late effect of cerebrovascular accident Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Scott syndrome Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Aplastic anemia co-occurrent with human immunodeficiency virus infection Has interpretation True Abnormal Inferred relationship Existential restriction modifier 8
Acquired epileptic aphasia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Acquired inhibitor of coagulation Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Pure red cell aplasia, acquired Has interpretation False Abnormal Inferred relationship Existential restriction modifier 7
Acquired stammering Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Ataxia pancytopenia syndrome Has interpretation False Abnormal Inferred relationship Existential restriction modifier 6
Platelet dysfunction caused by drugs Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Cellular immunologic aplastic anemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 8
Adductor spastic dysphonia of conversion reaction Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Resistance to activated protein C caused by Factor V Leiden Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Harlequin ichthyosis Has interpretation True Abnormal Inferred relationship Existential restriction modifier 4
Anticoagulant overdosage Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Thrombophilia caused by antineoplastic agent therapy Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Thrombophilia due to trauma Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Isolated collagen aggregation defect Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Thrombophilia due to myeloproliferative disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Thrombocytopenia caused by hypothermia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 4
Wiskott-Aldrich syndrome Has interpretation False Abnormal Inferred relationship Existential restriction modifier 3
Primary antiphospholipid syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Primary antiphospholipid syndrome with organ/system involvement Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Language disorder associated with right hemisphere damage Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Speech and language developmental delay due to hearing loss Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Primary antiphospholipid syndrome with multisystem involvement Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Secondary antiphospholipid syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Language disorder associated with thought disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Secondary antiphospholipid syndrome with organ/system involvement Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Secondary antiphospholipid syndrome with multisystem involvement Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Post-traumatic mutism Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Chronic idiopathic thrombocytopenic purpura Has interpretation True Abnormal Inferred relationship Existential restriction modifier 5
Language-related cognitive disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Aplastic anemia due to chronic disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 8
Hemorrhagic disease of the newborn due to factor II deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 4
Thrombophilia due to paroxysmal nocturnal hemoglobinuria Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Aplastic anemia due to infection Has interpretation False Abnormal Inferred relationship Existential restriction modifier 8
Aphasia due to brain damage Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Platelet secretory disorder Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Familial platelet syndrome with predisposition to acute myelogenous leukemia Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Aplastic anemia caused by radiation Has interpretation True Abnormal Inferred relationship Existential restriction modifier 8
Acute purpuric eruption of skin Has interpretation False Abnormal Inferred relationship Existential restriction modifier 4
Acquired factor VIII deficiency disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Acquired factor XI deficiency disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Metabolic purpura Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Acquired aplastic anemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 7
Netherton's syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Developmental and speech delay due to SRY-box 5 deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Perinatal thrombocytopenia Has interpretation False Abnormal Inferred relationship Existential restriction modifier 3
Congenital afibrinogenemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Childhood onset fluency disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Secondary aplastic anemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 7
Factor XI inhibitor disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Factor IX inhibitor disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Bleeding disorder due to glycoprotein VI deficiency Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Thrombophilia due to acquired antithrombin III deficiency Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Developmental motor speech disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Doan-Wright syndrome Has interpretation False Abnormal Inferred relationship Existential restriction modifier 6
Glanzmann's thrombasthenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Vagal hoarseness Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
X-linked congenital dyserythropoietic anemia with thrombocytopenia Has interpretation False Abnormal Inferred relationship Existential restriction modifier 7
Platelet procoagulant activity deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Antiphospholipid syndrome in pregnancy Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Bernard Soulier syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Induced termination of pregnancy complicated by afibrinogenemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Factor XIII inhibitor disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Aphonia paralytica Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Transient neonatal disorder of coagulation Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Warfarin overdosage Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Estren-Dameshek anemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 7
Thrombophilia caused by vascular device Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Thrombophilia due to immobilization Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Hypotrichosis and deafness syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Aplastic anemia caused by antineoplastic agent Has interpretation False Abnormal Inferred relationship Existential restriction modifier 7
Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Factor X inhibitor disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Antiphospholipid syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Congenital hypofibrinogenemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Ichthyosis hystrix Bäfverstedt type Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Hereditary factor IX deficiency disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Acquired afibrinogenemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Dystonia aphonia syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Congenital factor IX deficiency variant Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Purpura of skin co-occurrent and due to vascular fragility Has interpretation True Abnormal Inferred relationship Existential restriction modifier 4
Congenital factor IX deficiency with inhibitor Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Purpura of skin caused by mechanical force Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Congenital von Willebrand's disease Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Congenital von Willebrand's disease type I Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Acquired combined coagulation factor deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Pancytopenia with developmental delay syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 7
Congenital von Willebrand's disease type II Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Congenital von Willebrand's disease type III Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Disseminated intravascular coagulation due to placental abruption Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Acquired von Willebrand disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Akinetic mutism Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2

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