FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  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


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
Ataxic dysphonia Has interpretation True Abnormal Inferred relationship Some 1
Dissociative neurological symptom disorder with dysphonia (disorder) 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 False Abnormal Inferred relationship Some 1
Legal abortion with afibrinogenemia Has interpretation False Abnormal Inferred relationship Some 1
Developmental verbal dyspraxia Has interpretation True Abnormal Inferred relationship Some 1
MYH9 macrothrombocytopenia syndrome Has interpretation False 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 False 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 Has interpretation False 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 caused by drug therapy Has interpretation False 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 (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 False Abnormal Inferred relationship Some 3
On examination - speech delay 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 caused by aspirin (disorder) Has interpretation True Abnormal Inferred relationship Some 2

Start Previous Page 41 of 52 Next End


This concept is not in any reference sets

Back to Start