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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
Mild developmental articulation disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Ataxic dysphonia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Conversion dysphonia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Contact purpura Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Severe receptive language delay Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Homozygous protein C deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Speech and language disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Sex-linked thrombocytopenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Phonological disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Revesz syndrome Has interpretation False Abnormal Inferred relationship Existential restriction modifier 8
Mild hereditary factor VIII deficiency disease without inhibitor Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
von Willebrand disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Megakaryocytic thrombocytopenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Purpura pigmentosa chronica Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Acute hemorrhagic edema of childhood Has interpretation False Abnormal Inferred relationship Existential restriction modifier 3
Dysfluency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Semantic-pragmatic impairment Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Clothing purpura Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
von Willebrand disease, type IIH Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
Legal abortion with afibrinogenemia Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
Developmental verbal dyspraxia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
MYH9 macrothrombocytopenia syndrome Has interpretation False Abnormal Inferred relationship Existential restriction modifier 1
Secondary cutaneous vasculitis Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Afibrinogenemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Heterozygous protein C deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Thrombocytopenic purpura due to platelet consumption Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Severe hereditary factor IX deficiency disease without inhibitor Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Essential thrombocythemia Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Refractory thrombocytopenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Hereditary hyperhomocysteinemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hereditary factor XIII B subunit deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hereditary coagulation factor deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Transient neonatal thrombocytopenia due to isoimmunization Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Vitamin K deficiency coagulation disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Thrombophilia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Reactive thrombocytosis Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Homozygous Factor V Leiden mutation Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Coagulation factor deficiency syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Hypernasality and hyponasality Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
High bone mass osteogenesis imperfecta Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Hermansky-Pudlak syndrome Has interpretation False Abnormal Inferred relationship Existential restriction modifier 3
Osteogenesis imperfecta type I Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Ehlers-Danlos and osteogenesis imperfecta syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Osteogenesis imperfecta type III Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Osteogenesis imperfecta type IIA Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Osteogenesis imperfecta type II Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta Has interpretation True Abnormal Inferred relationship Existential restriction modifier 4
Osteogenesis imperfecta type IIB Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Osteogenesis imperfecta Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Osteogenesis imperfecta, type IV B Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Osteogenesis imperfecta type IV Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Osteoporosis with pseudoglioma Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 4
Osteogenesis imperfecta, type IV A Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Osteogenesis imperfecta, recessive perinatal lethal Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Osteogenesis imperfecta with blue sclerae AND normal teeth Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Osteogenesis imperfecta, dominant perinatal lethal Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Ichthyosis, short stature, brachydactyly, microspherophakia syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 5
Hereditary hyperekplexia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Sporadic hyperekplexia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Irregular tear film Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Abnormal hair finding Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Sexual dysfunction caused by amfetamine and/or amfetamine derivative Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Acquired hemophilia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Palmoplantar keratoderma, spastic paralysis syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Hyperekplexia epilepsy syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Chronic instability of bilateral knee joints Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Chronic instability of bilateral knee joints Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Adult onset fluency disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Aplastic anemia due to drugs Has interpretation True Abnormal Inferred relationship Existential restriction modifier 8
Acquired factor V deficiency disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Systemic lupus erythematosus-associated antiphospholipid syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Perinatal purpura Has interpretation False Abnormal Inferred relationship Existential restriction modifier 3
Heparin-induced thrombocytopenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Bleeding diathesis due to thromboxane synthesis deficiency Has interpretation True Abnormal Inferred relationship Existential restriction modifier 4
Congenital factor IX deficiency without inhibitor Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Neonatal thrombocytopenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Bleeding diathesis due to collagen receptor defect Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Congenital plasminogen activator inhibitor deficiency type 1 Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Disorder of fluency Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Thrombophilia due to acquired protein S deficiency Has interpretation False Abnormal Inferred relationship Existential restriction modifier 2
Thrombocytopenia due to hypersplenism Has interpretation False Abnormal Inferred relationship Existential restriction modifier 3
Speech and language deficit due to and following ischemic cerebrovascular accident Has interpretation False Abnormal Inferred relationship Existential restriction modifier 3
Immune thrombocytopenia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 4
Factor V inhibitor disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Acquired factor X deficiency disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Thrombophilia caused by drug therapy Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Pancytopenia caused by medication Has interpretation True Abnormal Inferred relationship Existential restriction modifier 1
Congenital auditory imperception Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Oligoovulatory dysfunctional uterine bleeding Has interpretation True Abnormal Inferred relationship Existential restriction modifier 4
Psychogenic stammering Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Hereditary dysfibrinogenemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Severe fever with thrombocytopenia syndrome virus Has interpretation True Abnormal Inferred relationship Existential restriction modifier 6
Immunologic aplastic anemia Has interpretation True Abnormal Inferred relationship Existential restriction modifier 7
Vascular hemostatic disease Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Childhood and adolescent disturbance with elective mutism Has interpretation False Abnormal Inferred relationship Existential restriction modifier 3
On examination - speech delay Has interpretation False Abnormal Inferred relationship Existential restriction modifier 4
Thrombocytopenia with acquired immunodeficiency syndrome Has interpretation True Abnormal Inferred relationship Existential restriction modifier 3
Acquired coagulation factor inhibitor disorder Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2
Hereditary combined deficiency of vitamin K-dependent clotting factors Has interpretation True Abnormal Inferred relationship Existential restriction modifier 2

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