FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  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
139711000077111 anormal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
2337331000195117 Abnorm de Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
2337341000195113 Auffällig de Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

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
Exhausted platelets Has interpretation True Abnormal Inferred relationship Some 1
Motor speech disorder Has interpretation True Abnormal Inferred relationship Some 1
Spastic pseudobulbar dysphonia Has interpretation True Abnormal Inferred relationship Some 1
Alpha-2-antiplasmin deficiency Has interpretation True Abnormal Inferred relationship Some 1
Disorder of speech and language development Has interpretation True Abnormal Inferred relationship Some 1
Postpartum coagulation defect with hemorrhage Has interpretation True Abnormal Inferred relationship Some 2
Autoimmune neonatal thrombocytopenia Has interpretation False Abnormal Inferred relationship Some 3
Organic amnesia of language (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Blood coagulation disorder with impaired clot retraction time Has interpretation True Abnormal Inferred relationship Some 1
Adductor spastic dysphonia Has interpretation True Abnormal Inferred relationship Some 1
Afibrinogenemia following molar AND/OR ectopic pregnancy Has interpretation False Abnormal Inferred relationship Some 1
Oral dyspraxia Has interpretation True Abnormal Inferred relationship Some 1
Factor XI deficiency, type II Has interpretation True Abnormal Inferred relationship Some 1
Semantic impairment Has interpretation True Abnormal Inferred relationship Some 1
Speech and phonology impairments Has interpretation True Abnormal Inferred relationship Some 1
Hereditary factor IX deficiency disease without inhibitor (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Mixed transcortical dysphasia Has interpretation True Abnormal Inferred relationship Some 1
Megakaryocytic aplasia Has interpretation False Abnormal Inferred relationship Some 2
Neonatal thrombocytopenia due to platelet alloimmunization (disorder) Has interpretation True Abnormal Inferred relationship Some 2
maladie de von Willebrand type 2A Has interpretation False Abnormal Inferred relationship Some 1
Heterozygous prothrombin G20210A mutation (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Hemorrhagic disorder due to increase in anti-11a Has interpretation True Abnormal Inferred relationship Some 1
Fibrinolytic bleeding syndrome Has interpretation True Abnormal Inferred relationship Some 1
Purpura annularis telangiectodes of Majocchi Has interpretation True Abnormal Inferred relationship Some 3
Induced termination of pregnancy complicated by defibrination syndrome (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Phonological syntactic disorder Has interpretation True Abnormal Inferred relationship Some 1
Senile purpura Has interpretation True Abnormal Inferred relationship Some 2
A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by moderate to severe intellectual disability, congenital aphonia, hearing loss, optic atrophy, retinal dystrophy, broad thumbs and duplicated halluces. Facial dysmorphism (including thick eyebrows, ptosis, long, downslanting palpebral fissures, microstomia, low-set, posteriorly rotated ears) and genital abnormalities are also associated. Has interpretation True Abnormal Inferred relationship Some 4
Familial multiple factor deficiency syndrome, type II Has interpretation True Abnormal Inferred relationship Some 1
Developmental speech disorder Has interpretation True Abnormal Inferred relationship Some 1
Hyperkinetic dysphonia Has interpretation True Abnormal Inferred relationship Some 1
Limited sound system Has interpretation True Abnormal Inferred relationship Some 1
Qualitative platelet disorder (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Constitutional aplastic anemia with malformation Has interpretation True Abnormal Inferred relationship Some 6
Factor VIII deficiency Has interpretation True Abnormal Inferred relationship Some 1
Combined coagulation factor deficiency Has interpretation True Abnormal Inferred relationship Some 1
Velar dyspraxia Has interpretation True Abnormal Inferred relationship Some 1
fibrinolyse pendant le postpartum Has interpretation False Abnormal Inferred relationship Some 1
Mild expressive language delay Has interpretation True Abnormal Inferred relationship Some 1
Hereditary factor IX deficiency disease with inhibitor (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Hereditary factor XIII deficiency disease Has interpretation True Abnormal Inferred relationship Some 1
Familial multiple factor deficiency syndrome, type IV Has interpretation True Abnormal Inferred relationship Some 1
Classic onset hemorrhagic disease of newborn due to vitamin K deficiency Has interpretation True Abnormal Inferred relationship Some 2
Hereditary elevated factor XI (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Expressive language delay Has interpretation True Abnormal Inferred relationship Some 1
Developmental aphasia Has interpretation True Abnormal Inferred relationship Some 1
Factitious purpura Has interpretation False Abnormal Inferred relationship Some 2
Embolic purpura Has interpretation True Abnormal Inferred relationship Some 2
Severe hereditary factor VIII deficiency disease without inhibitor (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Miscarriage with afibrinogenemia (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Autoimmune pancytopenia Has interpretation False Abnormal Inferred relationship Some 5
Posttransfusion purpura Has interpretation True Abnormal Inferred relationship Some 3
Acoustic analysis deficit Has interpretation True Abnormal Inferred relationship Some 1
Systemic fibrinogenolysis Has interpretation True Abnormal Inferred relationship Some 1
This syndrome is extremely rare and is characterized by delayed speech development, mild facial asymmetry, strabismus and transverse ear lobe creases. Has interpretation True Abnormal Inferred relationship Some 2
Hereditary combined coagulation factor deficiency (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Anterior dysphasia Has interpretation True Abnormal Inferred relationship Some 1
Postpartum coagulation defects - delivered with postnatal problem Has interpretation False Abnormal Inferred relationship Some 1
Hereditary antithrombin III deficiency (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Thrombophilia associated with pregnancy Has interpretation True Abnormal Inferred relationship Some 1
syndrome des plaquettes Québec Has interpretation False Abnormal Inferred relationship Some 1
Phonological delay Has interpretation True Abnormal Inferred relationship Some 1
Acquired language disorder Has interpretation True Abnormal Inferred relationship Some 1
Normal non-fluency Has interpretation True Abnormal Inferred relationship Some 1
Hereditary hyperfibrinogenemia (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Abductor spastic dysphonia Has interpretation True Abnormal Inferred relationship Some 1
Moderate hereditary factor VIII deficiency disease with inhibitor (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Expressive language disorder Has interpretation True Abnormal Inferred relationship Some 1
Thrombocytopathy, asplenia and miosis (disorder) Has interpretation False Abnormal Inferred relationship Some 3
Hypofibrinogenemia Has interpretation True Abnormal Inferred relationship Some 1
Neonatal thrombocytopenia associated with maternal idiopathic thrombocytopenic purpura Has interpretation False Abnormal Inferred relationship Some 2
Developmental receptive language disorder (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Thrombotic thrombocytopenic purpura Has interpretation True Abnormal Inferred relationship Some 8
Hyperheparinemia Has interpretation True Abnormal Inferred relationship Some 1
Hereditary elevated factor VIII (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Hypofunctional dysphonia Has interpretation True Abnormal Inferred relationship Some 1
Non-contrastive sound system Has interpretation True Abnormal Inferred relationship Some 1
Dysplasminogenemia Has interpretation True Abnormal Inferred relationship Some 1
Neurologic voice disorder Has interpretation True Abnormal Inferred relationship Some 1
Mild receptive language delay Has interpretation True Abnormal Inferred relationship Some 1
Hereditary factor VII deficiency disease (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Pregnancy-related factor VIII deficiency Has interpretation True Abnormal Inferred relationship Some 1
Dysphonia of organic tremor Has interpretation True Abnormal Inferred relationship Some 1
à l'examen : dysphonie Has interpretation False Abnormal Inferred relationship Some 1
Eczematid-like purpura of Doucas and Kapetanakis Has interpretation True Abnormal Inferred relationship Some 4
Hereditary factor XII deficiency disease Has interpretation True Abnormal Inferred relationship Some 1
Waldenstrom's hypergammaglobulinaemic purpura Has interpretation True Abnormal Inferred relationship Some 2
Tongue tip dyspraxia Has interpretation True Abnormal Inferred relationship Some 1
Acquired platelet function disorder (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Dysproteinemic purpura (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Afibrinogenaemia - postpartum Has interpretation True Abnormal Inferred relationship Some 1
Developmental articulatory dyspraxia Has interpretation True Abnormal Inferred relationship Some 1
Hereditary factor VIII deficiency disease Has interpretation True Abnormal Inferred relationship Some 1
Purpuric disorder (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Auditory discrimination aphasia Has interpretation True Abnormal Inferred relationship Some 1
Severe hereditary factor VIII deficiency disease with inhibitor (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Developmental language comprehension impairment (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Factor XI deficiency, type I Has interpretation True Abnormal Inferred relationship Some 1
von Willebrand disease, type IIG Has interpretation False Abnormal Inferred relationship Some 1
Legal abortion with defibrination syndrome Has interpretation False Abnormal Inferred relationship Some 1
Developmental speech fluency disorder (disorder) Has interpretation True Abnormal Inferred relationship Some 1

Start Previous Page 39 of 56 Next End

This concept is not in any reference sets

Back to Start