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
Ataxic dysphonia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Conversion dysphonia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Contact purpura (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Severe receptive language delay	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Homozygous protein C deficiency (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Speech and language disorder	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Sex-linked thrombocytopenia	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Phonological disorder	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Revesz syndrome (disorder)	Has interpretation	False	Abnormal	Inferred relationship	Some	8
Mild hereditary factor VIII deficiency disease without inhibitor (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
von Willebrand disorder	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Megakaryocytic thrombocytopenia	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Purpura pigmentosa chronica	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Acute haemorrhagic oedema of childhood	Has interpretation	False	Abnormal	Inferred relationship	Some	3
Dysfluency	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Semantic-pragmatic impairment	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Clothing purpura (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	2
von Willebrand disease, type IIH	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Legal abortion with afibrinogenemia (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Developmental verbal dyspraxia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
MYH9 macrothrombocytopenia syndrome (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Secondary cutaneous vasculitis (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	3
Afibrinogenemia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Heterozygous protein C deficiency (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Thrombocytopenic purpura due to platelet consumption (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	3
Severe hereditary factor IX deficiency disease without inhibitor (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Essential thrombocythemia (disorder)	Has interpretation	False	Abnormal	Inferred relationship	Some	2
Refractory thrombocytopenia (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	3
Hereditary hyperhomocysteinemia (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Hereditary factor XIII B subunit deficiency (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Hereditary coagulation factor deficiency	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Transient neonatal thrombocytopenia due to isoimmunisation	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Vitamin K deficiency coagulation disorder	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Thrombophilia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Reactive thrombocytosis	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Homozygous Factor V Leiden mutation	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Coagulation factor deficiency syndrome	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Hypernasality and hyponasality	Has interpretation	True	Abnormal	Inferred relationship	Some	1
High bone mass osteogenesis imperfecta	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Hermansky-Pudlak syndrome	Has interpretation	False	Abnormal	Inferred relationship	Some	3
Osteogenesis imperfecta type I (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Ehlers-Danlos and osteogenesis imperfecta syndrome	Has interpretation	True	Abnormal	Inferred relationship	Some	3
Osteogenesis imperfecta type III (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Osteogenesis imperfecta type IIA	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Osteogenesis imperfecta, perinatal lethal	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta	Has interpretation	True	Abnormal	Inferred relationship	Some	4
Osteogenesis imperfecta type IIB	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Osteogenesis imperfecta	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Osteogenesis imperfecta, type IV B	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Osteogenesis imperfecta with normal sclerae, dominant form	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Osteoporosis with pseudoglioma	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	4
Osteogenesis imperfecta, type IV A (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Osteogenesis imperfecta, recessive perinatal lethal	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Osteogenesis imperfecta with blue sclerae AND normal teeth	Has interpretation	True	Abnormal	Inferred relationship	Some	3
Osteogenesis imperfecta, dominant perinatal lethal	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Ichthyosis, short stature, brachydactyly, microspherophakia syndrome	Has interpretation	True	Abnormal	Inferred relationship	Some	5
Hereditary hyperekplexia (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	3
Sporadic hyperekplexia (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Irregular tear film (finding)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Abnormal hair finding (finding)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Sexual dysfunction caused by amfetamine and/or amfetamine derivative (finding)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Acquired hemophilia	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Palmoplantar keratoderma, spastic paralysis syndrome (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Hyperekplexia epilepsy syndrome (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Chronic instability of bilateral knee joints	Has interpretation	False	Abnormal	Inferred relationship	Some	2
Chronic instability of bilateral knee joints	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Adult onset fluency disorder	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Aplastic anemia due to drugs	Has interpretation	True	Abnormal	Inferred relationship	Some	8
Acquired factor V deficiency disease	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Systemic lupus erythematosus-associated antiphospholipid syndrome (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	3
Perinatal purpura	Has interpretation	True	Abnormal	Inferred relationship	Some	3
Heparin-induced thrombocytopenia	Has interpretation	True	Abnormal	Inferred relationship	Some	3
Bleeding diathesis due to thromboxane synthesis deficiency	Has interpretation	True	Abnormal	Inferred relationship	Some	4
Congenital factor IX deficiency without inhibitor (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Neonatal thrombocytopenia	Has interpretation	True	Abnormal	Inferred relationship	Some	3
Bleeding diathesis due to collagen receptor defect	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Congenital plasminogen activator inhibitor deficiency type 1 (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Disorder of fluency	Has interpretation	False	Abnormal	Inferred relationship	Some	2
Thrombophilia due to acquired protein S deficiency (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Thrombocytopenia due to hypersplenism	Has interpretation	False	Abnormal	Inferred relationship	Some	3
Speech and language deficit due to and following ischemic cerebrovascular accident (disorder)	Has interpretation	False	Abnormal	Inferred relationship	Some	3
Immune thrombocytopenia	Has interpretation	True	Abnormal	Inferred relationship	Some	4
Factor V inhibitor disorder	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Acquired factor X deficiency disease	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Thrombophilia due to drug therapy	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Pancytopenia caused by medication (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	1
Congenital auditory imperception	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Oligoovulatory dysfunctional uterine bleeding (finding)	Has interpretation	True	Abnormal	Inferred relationship	Some	4
Psychogenic stammering	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Hereditary dysfibrinogenemia (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Severe fever with thrombocytopenia syndrome virus (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	6
Immunologic aplastic anemia	Has interpretation	True	Abnormal	Inferred relationship	Some	7
Vascular hemostatic disease	Has interpretation	True	Abnormal	Inferred relationship	Some	3
Childhood and adolescent disturbance with elective mutism	Has interpretation	True	Abnormal	Inferred relationship	Some	3
vid undersökning: talförsening	Has interpretation	False	Abnormal	Inferred relationship	Some	4
Thrombocytopenia with acquired immunodeficiency syndrome (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	3
Acquired coagulation factor inhibitor disorder (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder)	Has interpretation	True	Abnormal	Inferred relationship	Some	2
Platelet dysfunction due to aspirin	Has interpretation	True	Abnormal	Inferred relationship	Some	2

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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)