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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
Legal abortion with defibrination syndrome Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
Developmental speech fluency disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Combined deficiency of factor V and factor VIII Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Myosin heavy chain 9 non muscle related disease Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Verbal dyspraxia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hereditary von Willebrand disease type 2N Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Grapheme-phoneme conversion deficit Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Thrombocytosis Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Central auditory processing disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Amegakaryocytic thrombocytopenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Conversational disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Postpartum coagulation defects with postnatal problem Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Familial thrombomodulin anomalies Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Lexical syntactic disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Familial multiple factor deficiency syndrome, type V Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Dense body defect Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Transient neonatal thrombocytopenia due to exchange transfusion Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Restricted expressive language development Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Prekallikrein deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Anticoagulant-induced bleeding Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Primary thrombocytopenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Fluency disorder as sequela of cerebrovascular disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Disseminated intravascular coagulation in newborn Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Protein C deficiency disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hemorrhagic disorder due to circulating anticoagulants Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hypodysfibrinogenemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Developmental delay in receptive-expressive language Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Severe hereditary factor VIII deficiency disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hereditary von Willebrand disease type 1A Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Thrombocythemia with distal limb defect Has interpretation False Abnormal Inferred relationship Existential restriction modifier 4
Hyperfunctional dysphonia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Congenital amegakaryocytic thrombocytopenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Mild hereditary factor VIII deficiency disease with inhibitor Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hereditary dysplasminogenemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Oral apraxia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Idiopathic stammering Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Cognitive communication disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Transcortical sensory dysphasia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hereditary factor VIII deficiency disease with inhibitor Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Aplastic anemia associated with pregnancy Has interpretation False Abnormal Inferred relationship Existential restriction modifier 6
Purpura simplex Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Benign primary hypergammaglobulinemic purpura Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Mild hereditary factor VIII deficiency disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hereditary platelet function disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Postinfective immunoglobulin A vasculitis Has interpretation False Abnormal Inferred relationship Existential restriction modifier 3
Restricted receptive language development Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Mutational falsetto Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Blood coagulation disorder, categorized by value of screening test Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Flaccid dysphonia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Factor X deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Thrombocytopenic purpura due to defective platelet production Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Homozygous protein S deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Factor I deficiency disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Transient neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Thrombocytopenia due to non-immune destruction Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
A disintegrin and metalloproteinase with thrombospondin type 1 motif 13 deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Receptive language impairment Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
Defect of purinergic receptor p2y G protein-coupled 12 Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Developmental language disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Gray platelet syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Purpura rheumatica Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
von Willebrand disease, type IIC Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
Lupus anticoagulant disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Thrombocytopenic purpura associated with metabolic disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Phoneme-grapheme conversion deficit Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Antithrombin III deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
White platelet syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hereditary von Willebrand disease type 2M Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Conversion muteness Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
Restricted sound system Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Sociolinguistic disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Mixed dysphasia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Semantic-pragmatic disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hereditary heparin cofactor II deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Thromboxane generation defect Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hereditary von Willebrand disease type 2B Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
DK phocomelia syndrome Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Amegakaryocytic thrombocytopenia with congenital malformation Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Hereditary factor V deficiency disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Anti-factor II disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Anticoagulant excess without bleeding Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Elective mutism Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
von Willebrand disease type IA Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
Radial aplasia-thrombocytopenia syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Factor XIII deficiency disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Blood coagulation disorder due to liver disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Severe hereditary factor IX deficiency disease with inhibitor Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hemorrhagic disorder due to antithrombinemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Alpha chain defect dysfibrinogenemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Adductor spastic dysphonia of musculoskeletal tension reaction Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Familial multiple factor deficiency syndrome, type III Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Receptive language disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hyperkinetic aphonia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Conversion aphonia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Upshaw-Schulman syndrome Has interpretation False Abnormal Inferred relationship Existential restriction modifier 8
Congenital thrombocytopenic purpura Has interpretation False Abnormal Inferred relationship Existential restriction modifier 3
Hereditary von Willebrand disease type 1B Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Factor II deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Mild developmental articulation disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1

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