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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
Deficiency of naturally occurring coagulation factor inhibitor Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Giant platelet syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Factor XI deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Communication disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Dysphonia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Platelet membrane defect Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Discourse difficulties Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Blood coagulation disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Word finding difficulty Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hemorrhagic disorder due to increase in anti-9a Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Apraxic aphonia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Drug induced thrombotic thrombocytopenic purpura Has interpretation False Abnormal Inferred relationship Existential restriction modifier 8
von Willebrand disease, type 1^a^ Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
Cyclic thrombocytopenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Factor XI deficiency, type III Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Expressive language impairment Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
Acquired purpura fulminans Has interpretation True Abnormal Inferred relationship Existential restriction modifier 4
Prothrombin complex deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Moderate hereditary factor VIII deficiency disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Factor VII deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Illegal abortion with afibrinogenemia Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
Hereditary von Willebrand disease type 3 Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Blood coagulation disorder complicating pregnancy Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Severe expressive language delay Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hereditary hypoplasminogenemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Mixed receptive-expressive language disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Secondary thrombocytopenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Developmental language disorder co-occurrent with impairment of expressive language Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Idiopathic factor VIII deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Mixed alpha granule and dense body deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Stellate pseudoscar in senile purpura Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Hereditary factor II deficiency disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Secondary autoimmune thrombocytopenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Failed attempted abortion with defibrination syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Familial hemorrhagic diathesis Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Psychogenic vocal cord dysfunction Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Dermite ocre of Favre Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 4
Aphonia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
GATA binding protein 1 related thrombocytopenia with dyserythropoiesis Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Macrothrombocytopenia with mitral valve insufficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Semantic dysphasia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Failed attempted abortion with afibrinogenemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Blood coagulation disorder with prolonged bleeding time Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Mediterranean thrombocytopenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Periodontitis co-occurrent with Chédiak-Higashi syndrome Has interpretation False Abnormal Inferred relationship Existential restriction modifier 3
von Willebrand disease type 2M Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
Hereditary factor X deficiency disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Vocal abuse in children Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Dystonic dysphonia Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
von Willebrand disease type 2B Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
Speech and language dyspraxias Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Blood coagulation disorder complicating childbirth Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Familial multiple factor deficiency syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hemophilia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Chronic acquired pure red cell aplasia Has interpretation False Abnormal Inferred relationship Existential restriction modifier 6
Homozygous prothrombin G20210A mutation Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Familial multiple factor deficiency syndrome, type I Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Late onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Spastic aphonia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Steroid purpura Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Acquired factor IX deficiency disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hemorrhagic disorder due to increase in anti-10a Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Non-thrombocytopenic purpura Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Postpartum coagulation defects Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Postpartum fibrinolysis with hemorrhage Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Ventricular band phonation Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Acquired pancytopenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 5
von Willebrand disease, type IIE Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
Fibrinogen abnormality Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Miscarriage with defibrination syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
von Willebrand disease, type IIA Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
Antiprothrombin disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Capillary fragility abnormality Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Thrombocytopenia due to extracorporeal circulation of blood Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Articulatory dyspraxia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
von Willebrand disease, type IIF Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
Neonatal antiphospholipid syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Acquired platelet factor 3 disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Autosomal dominant deficiency of plasminogen Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
High molecular weight kininogen deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Developmental language disorder co-occurrent with impairment of mainly pragmatic language Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Psychogenic adductor spastic dysphonia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Pancytopenia-dysmelia Has interpretation False Abnormal Inferred relationship Existential restriction modifier 5
Autoimmune factor VIII deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Secondary non-thrombocytopenic purpura Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Platelet factor V deficiency (factor V Quebec) Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hyperglobulinemic purpura Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Dyspraxia of velopharynx Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hereditary thrombophilia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Cryofibrinogenemic purpura Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Immature articulatory praxis Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Immune thrombocytopenic purpura Has interpretation False Abnormal Inferred relationship Existential restriction modifier 4
Stasis purpura Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Purpura due to increased intravascular pressure Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Cryoglobulinemic purpura Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Heterozygous protein S deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Acquired red cell aplasia Has interpretation False Abnormal Inferred relationship Existential restriction modifier 6
Early onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Hereditary factor XIII A subunit deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1

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