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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
Progressive pigmentary dermatosis of Schamberg Has interpretation True Abnormal Inferred relationship Some 6
Solitary nodule of lung (finding) Has interpretation True Abnormal Inferred relationship Some 2
Single hyalinising granuloma of lung Has interpretation True Abnormal Inferred relationship Some 2
Psychogenic dysphonia Has interpretation True Abnormal Inferred relationship Some 1
Air hunger (finding) Has interpretation True Abnormal Inferred relationship Some 2
Psychogenic air hunger Has interpretation True Abnormal Inferred relationship Some 2
Disorder of placental circulatory function Has interpretation True Abnormal Inferred relationship Some 2
Abnormal placental secretion of chorionic gonadotropin Has interpretation True Abnormal Inferred relationship Some 2
Instability of prosthesis of right glenohumeral joint (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Instability of prosthesis of joint of left knee (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Instability of prosthesis of joint of right knee (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Instability of prosthesis of joint of left hip (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Instability of prosthesis of joint of right hip (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Instability of prosthesis of left glenohumeral joint (disorder) Has interpretation True Abnormal Inferred relationship Some 1
A rare genetic skin disease characterized by generalized skin peeling or superficial blisters without scarring, leukonychia, acral punctate keratoses coalescing into focal keratoderma on the weight-bearing areas, painful angular cheilitis, and knuckle pads with multiple hyperkeratotic micropapules. The skin appears dry and scaly with superficial exfoliation and underlying erythema. Histopathologic examination of affected skin areas is not specific and shows hyperkeratosis, acanthosis, and occasional intraepidermal clefting with irregular acantholysis. Has interpretation True Abnormal Inferred relationship Some 5
Plain X-ray of bone structure of rib abnormal (finding) Has interpretation True Abnormal Inferred relationship Some 1
Pale face Has interpretation True Abnormal Inferred relationship Some 3
Blue skin Has interpretation True Abnormal Inferred relationship Some 3
Cyanosis of skin Has interpretation True Abnormal Inferred relationship Some 3
Discoloration of skin Has interpretation True Abnormal Inferred relationship Some 2
Perinatal cyanotic attacks Has interpretation True Abnormal Inferred relationship Some 5
White discoloration of skin (finding) Has interpretation True Abnormal Inferred relationship Some 3
Different skin color in opposite limb (finding) Has interpretation True Abnormal Inferred relationship Some 2
Yellow skin Has interpretation True Abnormal Inferred relationship Some 3
Grey skin Has interpretation True Abnormal Inferred relationship Some 3
Dusky discoloration of skin (finding) Has interpretation True Abnormal Inferred relationship Some 2
Phlegmasia alba dolens in pregnancy (disorder) Has interpretation True Abnormal Inferred relationship Some 6
Phlegmasia alba dolens Has interpretation True Abnormal Inferred relationship Some 4
Phlegmasia alba dolens in puerperium (disorder) Has interpretation True Abnormal Inferred relationship Some 4
Cyanotic attack (finding) Has interpretation True Abnormal Inferred relationship Some 4
Hypercyanotic spell due to congenital heart disease Has interpretation True Abnormal Inferred relationship Some 5
Pale discoloration of entire skin of body (finding) Has interpretation True Abnormal Inferred relationship Some 3
Multidirectional instability of left glenohumeral joint (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Multidirectional instability of right glenohumeral joint (disorder) Has interpretation True Abnormal Inferred relationship Some 1
A rare genetic disease characterized by microcephaly, global developmental delay, intellectual disability, abnormal muscle tone, and sensorineural hearing impairment. Additional variable manifestations include epilepsy, cortical visual impairment, gastrointestinal disturbances, growth restriction, scoliosis, as well as immunodeficiency and thrombocytopenia. Brain imaging may show cerebral atrophy, thin corpus callosum, and hypomyelination. Has interpretation True Abnormal Inferred relationship Some 7
Multidirectional instability of glenohumeral joint (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Cyanosis Has interpretation True Abnormal Inferred relationship Some 4
Stokvis' disease Has interpretation True Abnormal Inferred relationship Some 5
Hemoglobinopathy with cyanosis Has interpretation True Abnormal Inferred relationship Some 5
Finding characterized by slowing of blood flow to a peripheral body region in association with an increase in oxygen extraction from normally saturated arterial blood. Has interpretation True Abnormal Inferred relationship Some 4
Neonatal cyanosis Has interpretation True Abnormal Inferred relationship Some 5
A form of cyanosis that occurs when there is a decrease in oxygen saturation in the arterial blood, usually with an SaO2 of below 75%. Has interpretation True Abnormal Inferred relationship Some 4
Pulmonary cyanosis Has interpretation True Abnormal Inferred relationship Some 5
Acrocyanosis Has interpretation True Abnormal Inferred relationship Some 4
Blue baby Has interpretation True Abnormal Inferred relationship Some 5
Neonatal acrocyanosis Has interpretation True Abnormal Inferred relationship Some 5
Traumatic neonatal facial cyanosis Has interpretation True Abnormal Inferred relationship Some 5
Diffuse palmoplantar keratoderma-acrocyanosis syndrome is characterized by the association of diffuse palmoplantar keratoderma and acrocyanosis. It has been described in eight members of one family and in two sporadic cases. The mode of inheritance in the familial cases was autosomal dominant. Has interpretation True Abnormal Inferred relationship Some 5
Cyanotic congenital heart disease Has interpretation True Abnormal Inferred relationship Some 5
Local cyanosis Has interpretation True Abnormal Inferred relationship Some 4
Generalized inflammatory peeling skin syndrome Has interpretation True Abnormal Inferred relationship Some 4
Generalized non-inflammatory peeling skin syndrome Has interpretation True Abnormal Inferred relationship Some 3
Instability of prosthesis of joint of hip (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Instability of prosthesis of joint of knee Has interpretation True Abnormal Inferred relationship Some 1
Instability of prosthesis of glenohumeral joint (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Increase in opacification of the lung which does not obscure the blood vessels and airways. Has interpretation True Abnormal Inferred relationship Some 2
Cyanosis of skin over lesion (finding) Has interpretation True Abnormal Inferred relationship Some 4
Ichthyosis hystrix gravior (disorder) Has interpretation True Abnormal Inferred relationship Some 2
X-linked intellectual disability-short stature-overweight syndrome is a multiple congenital anomalies syndrome characterised by borderline to severe intellectual disability, speech delay, short stature, elevated body mass index, a pattern of truncal obesity (reported in older males), and variable neurologic features (e.g. hypotonia, tremors, gait disturbances, behavioural problems, and seizure disorders). Less common manifestations include microcephaly, microorchidism and/or microphallus. Dysmorphic features have been reported in some patients but no consistent pattern has been noted. Has interpretation True Abnormal Inferred relationship Some 4
Acrodynia due to mercury poisoning Has interpretation True Abnormal Inferred relationship Some 3
Juvenile pityriasis rubra pilaris (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Acquired ichthyosis due to paraneoplastic syndrome (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Discoloration of skin of breast Has interpretation True Abnormal Inferred relationship Some 1
Adult pityriasis rubra pilaris Has interpretation True Abnormal Inferred relationship Some 2
Left corneal rust ring Has interpretation True Abnormal Inferred relationship Some 2
Right corneal rust ring Has interpretation True Abnormal Inferred relationship Some 2
Corneal rust ring Has interpretation True Abnormal Inferred relationship Some 2
Lung function testing abnormal Has interpretation True Abnormal Inferred relationship Some 1
Intrinsic staining of tooth due to and following dental trauma Has interpretation True Abnormal Inferred relationship Some 1
Intrinsic staining of vital tooth (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Extrinsic staining of vital tooth (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Upshaw-Schulman syndrome (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Pulse missed beats Has interpretation True Abnormal Inferred relationship Some 1
Pulse missed beats Has interpretation True Abnormal Inferred relationship Some 3
Coin lesion of lung Has interpretation True Abnormal Inferred relationship Some 2
Systolic heart failure stage B Has interpretation True Abnormal Inferred relationship Some 1
Diastolic heart failure stage B Has interpretation True Abnormal Inferred relationship Some 1
Systolic heart failure stage B due to ischemic cardiomyopathy (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Excessive uterine contraction Has interpretation True Abnormal Inferred relationship Some 2
Reduced uterine contraction Has interpretation True Abnormal Inferred relationship Some 2
Niggling uterine contractions Has interpretation True Abnormal Inferred relationship Some 2
Reversal of uterine contraction wave Has interpretation True Abnormal Inferred relationship Some 2
Fundal height high for dates (finding) Has interpretation True Abnormal Inferred relationship Some 2
Fundal height low for dates Has interpretation True Abnormal Inferred relationship Some 2
Inappropriate uterine contraction Has interpretation True Abnormal Inferred relationship Some 2
Premature uterine contraction Has interpretation True Abnormal Inferred relationship Some 2
Poor retraction of upper segment Has interpretation True Abnormal Inferred relationship Some 2
Excessive retraction of upper uterine segment Has interpretation True Abnormal Inferred relationship Some 2
A rare, inherited bleeding disorder characterized by defective platelet adhesion and secondary coagulation defect that manifests as abnormal bleeding of variable severity occurring either spontaneously or in association with an invasive procedure. Three main subtypes are defined based on the type of von Willebrand factor defect: partial (type 1) or total (type 3) deficiency, and qualitative/functional anomalies (type 2). Has interpretation True Abnormal Inferred relationship Some 1
Reversal of uterine contraction wave Has interpretation True Abnormal Inferred relationship Some 3
Placental infarct affecting management of mother Has interpretation True Abnormal Inferred relationship Some 3
Placental infarct Has interpretation True Abnormal Inferred relationship Some 3
Uterine contractions problem Has interpretation True Abnormal Inferred relationship Some 2
Local exogenous pigmentation of mucosa of hard palate (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Local exogenous pigmentation of mucosa of soft palate (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Local exogenous pigmentation of mucous membrane of upper lip (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Local exogenous pigmentation of mucous membrane of lower lip (disorder) Has interpretation True Abnormal Inferred relationship Some 2
Local exogenous pigmentation of oral mucosa Has interpretation True Abnormal Inferred relationship Some 2
A rare condition associated with acquired immunodeficiency syndrome (AIDS) and characterised by unwanted weight loss (involving both fat and muscle) of more than ten percent of body weight, with either diarrhoea or weakness and fever which have lasted at least 30 days and are not related to an infection. Has interpretation True Abnormal Inferred relationship Some 2
Hematopoietic subsyndrome of acute radiation syndrome (disorder) Has interpretation True Abnormal Inferred relationship Some 3
Terra firma-forme dermatosis (disorder) Has interpretation True Abnormal Inferred relationship Some 2

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