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
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 Willebrands sjukdom, typ 1a	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
nedsatt expressiv språkförmåga	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 abort med afibrinogenemi	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
akroangiodermatit	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
parodontit samtidigt med Chédiak-Higashis syndrom	Has interpretation	False	Abnormal	Inferred relationship	Some	3
von Willebrands sjukdom, typ 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
dyston dysfoni	Has interpretation	False	Abnormal	Inferred relationship	Some	1
von Willebrands sjukdom, typ 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 Willebrands sjukdom, typ 2E	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 Willebrands sjukdom, typ 2A	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 Willebrands sjukdom, typ 2F	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
pancytopeni-dysmeli	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
idiopatisk trombocytopen 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

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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)