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263654008: Abnormal (qualifier value)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

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

4 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
Hereditary elevated factor VIII Has interpretation True Abnormal Inferred relationship Some 1
Hypofunctional dysphonia Has interpretation True Abnormal Inferred relationship Some 1
Non-contrastive sound system Has interpretation True Abnormal Inferred relationship Some 1
Dysplasminogenaemia Has interpretation True Abnormal Inferred relationship Some 1
Neurologic voice disorder Has interpretation True Abnormal Inferred relationship Some 1
Mild receptive language delay Has interpretation True Abnormal Inferred relationship Some 1
Hereditary factor VII deficiency disease Has interpretation True Abnormal Inferred relationship Some 1
Pregnancy-related factor VIII deficiency Has interpretation True Abnormal Inferred relationship Some 1
Dysphonia of organic tremor Has interpretation True Abnormal Inferred relationship Some 1
O/E - dysphonia Has interpretation False Abnormal Inferred relationship Some 1
Eczematid-like purpura of Doucas and Kapetanakis Has interpretation True Abnormal Inferred relationship Some 4
Hereditary factor XII deficiency disease Has interpretation True Abnormal Inferred relationship Some 1
Waldenstrom's hypergammaglobulinaemic purpura Has interpretation True Abnormal Inferred relationship Some 2
Tongue tip dyspraxia Has interpretation True Abnormal Inferred relationship Some 1
Acquired platelet function disorder Has interpretation True Abnormal Inferred relationship Some 1
Dysproteinemic purpura Has interpretation True Abnormal Inferred relationship Some 2
Afibrinogenaemia - postpartum Has interpretation True Abnormal Inferred relationship Some 1
Developmental articulatory dyspraxia Has interpretation True Abnormal Inferred relationship Some 1
Hereditary factor VIII deficiency disease Has interpretation True Abnormal Inferred relationship Some 1
Purpuric disorder Has interpretation True Abnormal Inferred relationship Some 2
Auditory discrimination aphasia Has interpretation True Abnormal Inferred relationship Some 1
Severe hereditary factor VIII deficiency disease with inhibitor Has interpretation True Abnormal Inferred relationship Some 1
Developmental language comprehension impairment Has interpretation True Abnormal Inferred relationship Some 1
Factor XI deficiency, type I Has interpretation True Abnormal Inferred relationship Some 1
von Willebrand disease, type IIG Has interpretation False Abnormal Inferred relationship Some 1
Legal termination of pregnancy with defibrination syndrome Has interpretation False Abnormal Inferred relationship Some 1
Developmental speech fluency disorder Has interpretation True Abnormal Inferred relationship Some 1
Combined deficiency of factor V and factor VIII 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 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 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 Has interpretation True Abnormal Inferred relationship Some 1
Severe hereditary factor VIII deficiency disease Has interpretation True Abnormal Inferred relationship Some 1
Hereditary von Willebrand disease type IA Has interpretation True Abnormal Inferred relationship Some 1
Thrombocythaemia with distal limb defect Has interpretation False Abnormal Inferred relationship Some 4
Hyperfunctional dysphonia Has interpretation True Abnormal Inferred relationship Some 1
Congenital amegakaryocytic thrombocytopenia Has interpretation True Abnormal Inferred relationship Some 2
Mild hereditary factor VIII deficiency disease with inhibitor Has interpretation True Abnormal Inferred relationship Some 1
Hereditary dysplasminogenaemia Has interpretation True Abnormal Inferred relationship Some 1
Oral apraxia Has interpretation True Abnormal Inferred relationship Some 1
Idiopathic stuttering Has interpretation True Abnormal Inferred relationship Some 1
Cognitive communication 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 Has interpretation True Abnormal Inferred relationship Some 1
Aplastic anaemia associated with pregnancy Has interpretation False Abnormal Inferred relationship Some 6
Purpura simplex Has interpretation True Abnormal Inferred relationship Some 2
Benign primary hypergammaglobulinaemic purpura Has interpretation True Abnormal Inferred relationship Some 2
Mild hereditary factor VIII deficiency disease Has interpretation True Abnormal Inferred relationship Some 1
Hereditary platelet function disorder Has interpretation True Abnormal Inferred relationship Some 1
Postinfective immunoglobulin A vasculitis Has interpretation False Abnormal Inferred relationship Some 3
Restricted receptive language development Has interpretation True Abnormal Inferred relationship Some 1
Mutational falsetto Has interpretation True Abnormal Inferred relationship Some 1
Blood coagulation disorder, categorised 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 Has interpretation True Abnormal Inferred relationship Some 3
Homozygous protein S deficiency Has interpretation True Abnormal Inferred relationship Some 1
Factor I deficiency disease Has interpretation True Abnormal Inferred relationship Some 1
Transient neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia 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 (ADAMTS13) Has interpretation True Abnormal Inferred relationship Some 1
Receptive language impairment Has interpretation False Abnormal Inferred relationship Some 1
P2Y12 defect 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
Purpura rheumatica Has interpretation False Abnormal Inferred relationship Some 2
Haemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Has interpretation True Abnormal Inferred relationship Some 1
von Willebrand disease, type IIC Has interpretation False Abnormal Inferred relationship Some 1
Lupus anticoagulant disorder Has interpretation True Abnormal Inferred relationship Some 1
Thrombocytopenic purpura associated with metabolic 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 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 False 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 Has interpretation True Abnormal Inferred relationship Some 1
Thromboxane generation defect Has interpretation True Abnormal Inferred relationship Some 1

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