263654008: Abnormal (qualifier value)

SNOMED CT Concept\Qualifier value\Finding value (qualifier value)\Normality findings\Abnormal

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

163721000052110 abnorm sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

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
Developmental speech fluency disorder (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Combined deficiency of factor V and factor VIII (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
MYH9 related disease	Has interpretation	False	Abnormal	Inferred relationship	Some	2
Verbal dyspraxia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
von Willebrand disease type 2N	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Grapheme-phoneme conversion deficit	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Thrombocytosis	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Central auditory processing disorder	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Amegakaryocytic thrombocytopenia	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Conversational disorder	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Postpartum coagulation defects with postnatal problem	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Familial thrombomodulin anomalies (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Lexical syntactic disorder	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Familial multiple factor deficiency syndrome, type V	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Dense body defect	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Transient neonatal thrombocytopenia due to exchange transfusion	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Restricted expressive language development (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Prekallikrein deficiency	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Anticoagulant-induced bleeding	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Primary thrombocytopenia	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Fluency disorder as sequela of cerebrovascular disease	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Disseminated intravascular coagulation in newborn	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Protein C deficiency disease	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Hemorrhagic disorder due to circulating anticoagulants	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Hypodysfibrinogenaemia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Developmental delay in receptive-expressive language (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Severe hereditary factor VIII deficiency disease (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Hereditary von Willebrand disease type IA	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Thrombocythemia with distal limb defect (disorder)	Has interpretation	False	Abnormal	Inferred relationship	Some	4
Hyperfunctional dysphonia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Congenital amegakaryocytic thrombocytopenia (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Mild hereditary factor VIII deficiency disease with inhibitor (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Hereditary dysplasminogenemia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Oral apraxia (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Idiopathic stammering	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Cognitive communication disorder (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Transcortical sensory dysphasia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Hereditary factor VIII deficiency disease with inhibitor (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Aplastic anemia associated with pregnancy (disorder)	Has interpretation	False	Abnormal	Inferred relationship	Some	6
Purpura simplex	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Benign primary hypergammaglobulinemic purpura	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Mild hereditary factor VIII deficiency disease (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Hereditary platelet function disorder (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Postinfective immunoglobulin A vasculitis (disorder)	Has interpretation	False	Abnormal	Inferred relationship	Some	3
Restricted receptive language development	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Mutational falsetto (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Blood coagulation disorder, categorized by value of screening test	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Flaccid dysphonia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Factor X deficiency	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Thrombocytopenic purpura due to defective platelet production (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	3
Homozygous protein S deficiency (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Factor I deficiency disease (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Transient neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Thrombocytopenia due to non-immune destruction	Has interpretation	True	Abnormal	Inferred relationship	Some	2
A disintegrin and metalloproteinase with thrombospondin type 1 motif 13 deficiency (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Receptive language impairment	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Defect of purinergic receptor p2y G protein-coupled 12 (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Developmental language disorder	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Gray platelet syndrome	Has interpretation	True	Abnormal	Inferred relationship	Some	1
reumatisk purpura	Has interpretation	False	Abnormal	Inferred relationship	Some	2
Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation	Has interpretation	True	Abnormal	Inferred relationship	Some	1
von Willebrand disease, type IIC	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Lupus anticoagulant disorder	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Thrombocytopenic purpura associated with metabolic disorder (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	3
Phoneme-grapheme conversion deficit	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Antithrombin III deficiency	Has interpretation	True	Abnormal	Inferred relationship	Some	1
White platelet syndrome (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Hereditary von Willebrand disease type 2M	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Conversion muteness	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Restricted sound system	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Sociolinguistic disorder	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Mixed dysphasia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Semantic-pragmatic disorder	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Hereditary heparin cofactor II deficiency (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Thromboxane generation defect	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Hereditary von Willebrand disease type 2B	Has interpretation	True	Abnormal	Inferred relationship	Some	1
DK phocomelia syndrome (disorder)	Has interpretation	False	Abnormal	Inferred relationship	Some	2
Amegakaryocytic thrombocytopenia with congenital malformation	Has interpretation	True	Abnormal	Inferred relationship	Some	3
Hereditary factor V deficiency disease	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Anti-factor II disorder	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Anticoagulant excess without bleeding	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Elective mutism	Has interpretation	True	Abnormal	Inferred relationship	Some	1
von Willebrand disease type IA	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Radial aplasia-thrombocytopenia syndrome	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Factor XIII deficiency disease	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Blood coagulation disorder due to liver disease	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Severe hereditary factor IX deficiency disease with inhibitor (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Haemorrhagic disorder due to antithrombinaemia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Alpha chain defect dysfibrinogenemia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Adductor spastic dysphonia of musculoskeletal tension reaction	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Familial multiple factor deficiency syndrome, type III	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Receptive language disorder	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Hyperkinetic aphonia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Conversion aphonia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Upshaw-Schulman syndrome (disorder)	Has interpretation	False	Abnormal	Inferred relationship	Some	8
Congenital thrombocytopenic purpura	Has interpretation	True	Abnormal	Inferred relationship	Some	3
von Willebrand disease type IB (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Factor II deficiency	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Mild developmental articulation disorder	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Ataxic dysphonia	Has interpretation	True	Abnormal	Inferred relationship	Some	1

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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
163721000052110	abnorm	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)