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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
Afibrinogenemia following ectopic pregnancy (disorder) Has interpretation True Abnormal Inferred relationship Some 4
Defibrination syndrome following molar pregnancy Has interpretation True Abnormal Inferred relationship Some 1
Defibrination syndrome following ectopic pregnancy (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Paroxysmal choreoathetosis Has interpretation True Abnormal Inferred relationship Some 1
Choreoathetosis Has interpretation True Abnormal Inferred relationship Some 2
Paroxysmal nonkinesigenic dyskinesia (disorder) Has interpretation True Abnormal Inferred relationship Some 3
Paroxysmal kinesigenic dyskinesia (disorder) Has interpretation True Abnormal Inferred relationship Some 3
Infantile Convulsions and paroxysmal ChoreoAthetosis (ICCA) syndrome is a neurological condition characterised by the occurrence of seizures during the first year of life and choreoathetotic dyskinetic attacks during childhood or adolescence. Has interpretation True Abnormal Inferred relationship Some 4
Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Acquired choreiform dyspraxia Has interpretation True Abnormal Inferred relationship Some 6
A rare multiple congenital anomalies/dysmorphic syndrome characterized by profound intellectual disability, choreoathetosis, progressive spastic diplegia, progressive tapetoretinal degeneration with loss of retinal vessels, and glomerulopathy resulting in death late in the first or early in the second decade of life. Absence of the cerebellar granular layer has been reported. There have been no further descriptions in the literature since 1982. Has interpretation True Abnormal Inferred relationship Some 8
Chorea due to Huntington disease-like 3 (disorder) Has interpretation True Abnormal Inferred relationship Some 4
Chorea due to Huntington disease-like 2 (disorder) Has interpretation True Abnormal Inferred relationship Some 3
Chorea due to Huntington disease-like 1 (disorder) Has interpretation True Abnormal Inferred relationship Some 4
Chorea co-occurrent and due to Wilson disease (disorder) Has interpretation True Abnormal Inferred relationship Some 7
Chorea gravidarum Has interpretation True Abnormal Inferred relationship Some 4
Chronic progressive non-hereditary chorea Has interpretation True Abnormal Inferred relationship Some 4
Westphal-Strumpell syndrome Has interpretation True Abnormal Inferred relationship Some 6
Choreic cerebral palsy Has interpretation True Abnormal Inferred relationship Some 1
A form of dyskinetic cerebral palsy with a combination of chorea and athetosis; movements are irregular, but twisting and curving. Has interpretation True Abnormal Inferred relationship Some 2
A rare severe neurodegenerative disorder that is considered one of the phenocopies of Huntington Disease (HD) affecting patients of African descent and characterized by a triad of movement (chorea, oculomotor, parkinsonism), psychiatric (prominently sadness, irritability and anxiety), and cognitive abnormalities (early cognitive decline and subcortical-like dementia). Has interpretation True Abnormal Inferred relationship Some 2
Hemichorea Has interpretation True Abnormal Inferred relationship Some 3
Post-hemiplegic chorea Has interpretation True Abnormal Inferred relationship Some 1
Hemichorea due to injury of head (disorder) Has interpretation True Abnormal Inferred relationship Some 4
Hemichorea due to cerebral arteriovenous malformation (disorder) Has interpretation True Abnormal Inferred relationship Some 4
Hemichorea due to abscess of brain (disorder) Has interpretation True Abnormal Inferred relationship Some 4
Hemichorea due to cerebral hemorrhage (disorder) Has interpretation True Abnormal Inferred relationship Some 4
Hemichorea due to neoplasm of brain (disorder) Has interpretation True Abnormal Inferred relationship Some 4
Hemichorea due to cerebral infarction (disorder) Has interpretation True Abnormal Inferred relationship Some 4
Hemichorea due to multiple sclerosis (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Systemic exogenous pigmentation of oral mucosa Has interpretation True Abnormal Inferred relationship Some 2
Amalgam tattoo Has interpretation True Abnormal Inferred relationship Some 1
Exogenous pigmentation of oral mucosa Has interpretation True Abnormal Inferred relationship Some 2
Drug-induced oral pigmentation (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Digital breast tomosynthesis abnormal Has interpretation True Abnormal Inferred relationship Some 1
Acute ST segment elevation myocardial infarction of atrium Has interpretation True Abnormal Inferred relationship Some 2
Fluency disorder due to and following embolic cerebrovascular accident (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Acute ST segment elevation myocardial infarction due to occlusion of proximal portion of circumflex branch of left coronary artery (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Acute ST segment elevation myocardial infarction due to distal left circumflex coronary artery occlusion Has interpretation True Abnormal Inferred relationship Some 2
Acute ST segment elevation myocardial infarction due to obtuse marginal branch of left circumflex coronary artery occlusion Has interpretation True Abnormal Inferred relationship Some 2
Acute ST segment elevation myocardial infarction due to posterolateral branch of left circumflex coronary artery occlusion Has interpretation True Abnormal Inferred relationship Some 2
Acute ST segment elevation myocardial infarction due to mid left circumflex coronary artery occlusion Has interpretation True Abnormal Inferred relationship Some 2
Chorea due to injury of head (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Chorea following injury Has interpretation True Abnormal Inferred relationship Some 1
Postpartum hemolysis-elevated liver enzymes-low platelet count syndrome Has interpretation True Abnormal Inferred relationship Some 3
Fanconi anemia of complementation group C Has interpretation True Abnormal Inferred relationship Some 7
Mild hereditary factor VIII deficiency disease with high response inhibitor (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Mild hereditary factor VIII deficiency disease with low response inhibitor Has interpretation True Abnormal Inferred relationship Some 1
Severe hereditary factor VIII deficiency disease with high response inhibitor (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Severe hereditary factor VIII deficiency disease with low response inhibitor Has interpretation True Abnormal Inferred relationship Some 1
Moderate hereditary factor VIII deficiency disease with high response inhibitor Has interpretation True Abnormal Inferred relationship Some 1
Moderate hereditary factor VIII deficiency disease with low response inhibitor Has interpretation True Abnormal Inferred relationship Some 1
Severe hereditary factor IX deficiency disease with high response inhibitor Has interpretation True Abnormal Inferred relationship Some 1
Severe hereditary factor IX deficiency disease with low response inhibitor (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Moderate hereditary factor IX deficiency disease with high response inhibitor Has interpretation True Abnormal Inferred relationship Some 1
Moderate hereditary factor IX deficiency disease with low response inhibitor (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Mild hereditary factor IX deficiency disease with high response inhibitor Has interpretation True Abnormal Inferred relationship Some 1
Mild hereditary factor IX deficiency disease with low response inhibitor (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Pancytopenia caused by colchicine (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Pancytopenia caused by non-steroidal anti-inflammatory agent (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Tooth eruption disorder (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Altered passive eruption of teeth Has interpretation True Abnormal Inferred relationship Some 3
Failure of tooth eruption Has interpretation True Abnormal Inferred relationship Some 2
Overeruption of tooth Has interpretation True Abnormal Inferred relationship Some 2
Supereruption of unopposed tooth Has interpretation True Abnormal Inferred relationship Some 3
Supereruption of tooth associated with malocclusion Has interpretation True Abnormal Inferred relationship Some 3
Submerging tooth Has interpretation True Abnormal Inferred relationship Some 2
A tooth which erupts after birth in the neonatal period. Has interpretation True Abnormal Inferred relationship Some 2
Failure of tooth eruption associated with tooth impaction (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Late tooth eruption Has interpretation True Abnormal Inferred relationship Some 2
An ectopic tooth that has erupted on the lingual aspect of the maxilla or mandible. Has interpretation True Abnormal Inferred relationship Some 2
Trichodermodysplasia-dental alterations syndrome is a rare, genetic ectodermal dysplasia syndrome characterized by sparse, thin, brittle scalp hair, as well as sparse eyebrows, eyelashes, axillary and pubic hair, delayed eruption of deciduous teeth and hypodontia of both dentitions. Mild palmoplantar keratosis, café-au-lait spots on back, mild dystrophy of nails, and tibial deflection of toes are also associated. There have been no further descriptions in the literature since 1986. Has interpretation True Abnormal Inferred relationship Some 6
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome (disorder) Has interpretation True Abnormal Inferred relationship Some 7
Premature tooth eruption Has interpretation True Abnormal Inferred relationship Some 2
Natal tooth Has interpretation True Abnormal Inferred relationship Some 2
Obstructed tooth eruption Has interpretation True Abnormal Inferred relationship Some 2
Labial ectopic tooth Has interpretation True Abnormal Inferred relationship Some 2
A rare malformation syndrome characterized by generalized multiple steatocystomas and natal teeth. Has interpretation True Abnormal Inferred relationship Some 3
A rare ectodermal dysplasia syndrome characterized by neonatal teeth, trichodystrophy (with straw-like, discolored and fragile hair), onychodystrophy, and malformation of the hands and feet consisting of simian-like hands with transverse palmar creases and prominent interdigital folds, brachydactyly, and marked shortness of the first metacarpal and metatarsal bones with hypoplasia of the distal phalanges. There have been no further descriptions in the literature since 1997. Has interpretation True Abnormal Inferred relationship Some 4
Noneruption of teeth - maxillary hypoplasia - genu valgum is an extremely rare syndrome that is characterized by multiple unerupted permanent teeth, hypoplasia of the alveolar process and of the maxillo-zygomatic region, severe genu valgum and deformed ears. Has interpretation True Abnormal Inferred relationship Some 5
Natal teeth (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Delayed generalised tooth eruption due to systemic disease Has interpretation True Abnormal Inferred relationship Some 3
A rare genetic odontologic disease characterized by failure of eruption of non-ankylosed permanent teeth without evidence of obvious mechanical obstruction. Posterior teeth are preferentially affected (typically with involvement of all teeth distal to the most mesial non-erupted tooth), resulting in a posterior open bite. Non-ankylosed teeth tend to become ankylosed, and orthodontic treatment of affected teeth is generally unsuccessful. Has interpretation True Abnormal Inferred relationship Some 2
Infraocclusion of tooth due to and following dental trauma (disorder) Has interpretation True Abnormal Inferred relationship Some 4
Disorder of eruption of permanent tooth due to and following dental trauma (disorder) Has interpretation True Abnormal Inferred relationship Some 4
Plain X-ray of soft tissue abnormal (finding) Has interpretation True Abnormal Inferred relationship Some 1
Plain X-ray of toe abnormal Has interpretation True Abnormal Inferred relationship Some 1
Plain X-ray of finger abnormal (finding) Has interpretation True Abnormal Inferred relationship Some 1
Plain X-ray of thumb abnormal (finding) Has interpretation True Abnormal Inferred relationship Some 1
Plain X-ray of fibula abnormal Has interpretation True Abnormal Inferred relationship Some 1
Plain X-ray of tibia abnormal (finding) Has interpretation True Abnormal Inferred relationship Some 1
Plain X-ray of lower leg abnormal (finding) Has interpretation True Abnormal Inferred relationship Some 1
Plain X-ray of bone of lower leg abnormal (finding) Has interpretation True Abnormal Inferred relationship Some 1
Misophonia (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Plain X-ray of humerus and bone of shoulder girdle abnormal (finding) Has interpretation True Abnormal Inferred relationship Some 1
Plain X-ray of radius and ulna abnormal Has interpretation True Abnormal Inferred relationship Some 1
Plain X-ray of forearm abnormal Has interpretation True Abnormal Inferred relationship Some 1
Plain X-ray of lower limb abnormal (finding) Has interpretation True Abnormal Inferred relationship Some 1
Plain X-ray of lumbar and sacral spine abnormal Has interpretation True Abnormal Inferred relationship Some 1
Plain X-ray of sacral spine abnormal Has interpretation True Abnormal Inferred relationship Some 1
Plain X-ray of oral soft tissue abnormal Has interpretation True Abnormal Inferred relationship Some 1

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