FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.5  |  FHIR Version n/a  User: [n/a]

263654008: Abnormal (qualifier value)


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


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

Start Previous Page 38 of 54 Next End


This concept is not in any reference sets

Back to Start