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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
Chronic instability of knee Has interpretation True Abnormal Inferred relationship Some 1
Finger joint unstable Has interpretation True Abnormal Inferred relationship Some 1
Meniscus unstable Has interpretation True Abnormal Inferred relationship Some 1
Hip unstable Has interpretation True Abnormal Inferred relationship Some 1
Temporomandibular joint unstable Has interpretation True Abnormal Inferred relationship Some 1
Chronic instability of joint Has interpretation True Abnormal Inferred relationship Some 1
Unstable knee Has interpretation True Abnormal Inferred relationship Some 1
Spinal instability Has interpretation True Abnormal Inferred relationship Some 1
Ankle instability Has interpretation True Abnormal Inferred relationship Some 1
Medial collateral ligament instability Has interpretation True Abnormal Inferred relationship Some 1
Lateral collateral ligament instability Has interpretation True Abnormal Inferred relationship Some 1
Instability of lumbosacral joint Has interpretation True Abnormal Inferred relationship Some 1
Toe joint unstable (finding) Has interpretation True Abnormal Inferred relationship Some 1
Instability of joint of left ankle (finding) Has interpretation True Abnormal Inferred relationship Some 1
Chronic ankle instability (finding) Has interpretation True Abnormal Inferred relationship Some 1
Elbow joint unstable Has interpretation True Abnormal Inferred relationship Some 1
Posterior cruciate instability Has interpretation True Abnormal Inferred relationship Some 1
Instability of right sacroiliac joint Has interpretation True Abnormal Inferred relationship Some 1
Cervicothoracic instability Has interpretation True Abnormal Inferred relationship Some 1
Acute ankle instability Has interpretation True Abnormal Inferred relationship Some 1
Wrist joint unstable Has interpretation True Abnormal Inferred relationship Some 1
Instability of foot joint (finding) Has interpretation True Abnormal Inferred relationship Some 1
Recurrent instability of joint Has interpretation True Abnormal Inferred relationship Some 1
Instability of joint of pelvis (finding) Has interpretation True Abnormal Inferred relationship Some 1
Anterior cruciate instability Has interpretation True Abnormal Inferred relationship Some 1
Instability of left sacroiliac joint Has interpretation True Abnormal Inferred relationship Some 1
Pivot shift test - instability Has interpretation True Abnormal Inferred relationship Some 1
Bilateral unstable hip Has interpretation False Abnormal Inferred relationship Some 1
Thumb joint unstable Has interpretation True Abnormal Inferred relationship Some 1
Instability of atlantooccipital joint Has interpretation True Abnormal Inferred relationship Some 1
Sacroiliac instability Has interpretation True Abnormal Inferred relationship Some 1
Instability of hand joint (finding) Has interpretation True Abnormal Inferred relationship Some 1
Subluxatable hip Has interpretation True Abnormal Inferred relationship Some 1
Dislocatable hip Has interpretation True Abnormal Inferred relationship Some 1
Congenital instability of hip joint Has interpretation True Abnormal Inferred relationship Some 1
Nail regrowth due to and following chemical destruction of nail bed Has interpretation True Abnormal Inferred relationship Some 1
Sweet smelling urine (finding) Has interpretation True Abnormal Inferred relationship Some 1
Lack of ossification of supraoccipital bone Has interpretation True Abnormal Inferred relationship Some 3
Lack of ossification of basioccipital bone Has interpretation True Abnormal Inferred relationship Some 3
Delayed epiphyseal closure Has interpretation False Abnormal Inferred relationship Some 1
Premature epiphyseal closure Has interpretation False Abnormal Inferred relationship Some 1
Lack of ossification of tympanic anulus Has interpretation True Abnormal Inferred relationship Some 3
Lack of ossification of squamosal bone Has interpretation True Abnormal Inferred relationship Some 3
Lack of ossification of alisphenoid bone Has interpretation True Abnormal Inferred relationship Some 3
Bone turnover rate disorder Has interpretation True Abnormal Inferred relationship Some 2
Bone turnover rate decreased Has interpretation False Abnormal Inferred relationship Some 1
Lack of ossification of zygomatic bone Has interpretation True Abnormal Inferred relationship Some 3
Increased bone formation Has interpretation False Abnormal Inferred relationship Some 2
Lack of ossification of frontal bone Has interpretation True Abnormal Inferred relationship Some 3
Craniolenticulosutural dysplasia (CLSD), also known as Boyadjiev-Jabs syndrome, is characterized by the specific association of large and late-closing fontanels, hypertelorism, early-onset cataract and mild generalized skeletal dysplasia. Has interpretation False Abnormal Inferred relationship Some 4
Bone resorption disorder Has interpretation False Abnormal Inferred relationship Some 2
Enlarged parietal foramina (EPF) is a developmental defect, characterized by variable intramembranous ossification defects of the parietal bones, which is either asymptomatic, symptomatic (headaches, nausea, vomiting, intellectual disability) or associated with other pathologies. Has interpretation True Abnormal Inferred relationship Some 2
Defect of skull ossification Has interpretation True Abnormal Inferred relationship Some 2
Lack of ossification of vomer Has interpretation True Abnormal Inferred relationship Some 3
Lack of ossification of basisphenoid bone Has interpretation True Abnormal Inferred relationship Some 3
Decreased maintenance of bone matrix Has interpretation False Abnormal Inferred relationship Some 1
Bone turnover rate increased Has interpretation False Abnormal Inferred relationship Some 1
Lack of ossification of interparietal bone Has interpretation True Abnormal Inferred relationship Some 3
Lack of ossification of nasal bone Has interpretation True Abnormal Inferred relationship Some 3
Lack of ossification of lacrimal bone Has interpretation True Abnormal Inferred relationship Some 3
Lack of ossification of maxilla Has interpretation True Abnormal Inferred relationship Some 3
épiphyse soudée Has interpretation False Abnormal Inferred relationship Some 2
Bone turnover rate absent Has interpretation False Abnormal Inferred relationship Some 1
Late closure of anterior fontanel Has interpretation False Abnormal Inferred relationship Some 1
Decreased osteoblast function Has interpretation False Abnormal Inferred relationship Some 1
Lack of ossification of exoccipital bone Has interpretation True Abnormal Inferred relationship Some 3
Lack of ossification of palatine bone Has interpretation True Abnormal Inferred relationship Some 3
Lack of ossification of parietal bone Has interpretation True Abnormal Inferred relationship Some 3
Incomplete ossification of interparietal bone Has interpretation True Abnormal Inferred relationship Some 2
Lack of bone formation Has interpretation False Abnormal Inferred relationship Some 2
Lack of ossification of premaxilla Has interpretation True Abnormal Inferred relationship Some 3
Osteoid formation disorder Has interpretation False Abnormal Inferred relationship Some 2
Lack of ossification of presphenoid bone Has interpretation True Abnormal Inferred relationship Some 3
Epiphysis formation disorder Has interpretation False Abnormal Inferred relationship Some 2
Early fontanel closure Has interpretation False Abnormal Inferred relationship Some 1
Functional bone disorder Has interpretation False Abnormal Inferred relationship Some 2
Reduced ossification Has interpretation False Abnormal Inferred relationship Some 1
Late fontanel closure Has interpretation False Abnormal Inferred relationship Some 1
Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome is a rare, genetic, syndromic intellectual disability disorder characterised by severe intellectual disability with significant speech and language impairment, hypohidrosis (often resulting in hyperthermia) with normal sweat gland appearance, tooth enamel hypoplasia, palmoplantar hyperkeratosis and a high frequency of acquired microcephaly. Mild facial dysmorphism, including lateral flaring of the eyebrows, broad nasal tip, and thick vermilion border, may also be observed. Has interpretation False Abnormal Inferred relationship Some 1
A rare ophthalmic disorder characterized by corneal opacification and dyskeratosis (which may cause visual impairment), associated with systemic features including palmoplantar hyperkeratosis, laryngeal dyskeratosis, pruritic hyperkeratotic scars, chronic rhinitis, dyshidrosis and/or nail thickening. Has interpretation True Abnormal Inferred relationship Some 1
Leukokeratosis of skin Has interpretation True Abnormal Inferred relationship Some 2
Leukokeratosis (disorder) Has interpretation True Abnormal Inferred relationship Some 1
Chronic instability of right knee joint Has interpretation True Abnormal Inferred relationship Some 1
Chronic instability of left knee joint Has interpretation True Abnormal Inferred relationship Some 1
Instability of bilateral patellofemoral joints (finding) Has interpretation True Abnormal Inferred relationship Some 1
Instability of bilateral hip joints (finding) Has interpretation True Abnormal Inferred relationship Some 1
Instability of right patellofemoral joint (finding) Has interpretation True Abnormal Inferred relationship Some 1
Instability of bilateral shoulder joints (finding) Has interpretation True Abnormal Inferred relationship Some 1
Instability of left patellofemoral joint (finding) Has interpretation True Abnormal Inferred relationship Some 1
Instability of right elbow joint (finding) Has interpretation True Abnormal Inferred relationship Some 1
Instability of right hip joint (finding) Has interpretation True Abnormal Inferred relationship Some 1
Instability of left hip joint (finding) Has interpretation True Abnormal Inferred relationship Some 1
Instability of right shoulder joint Has interpretation True Abnormal Inferred relationship Some 1
Instability of left shoulder joint Has interpretation True Abnormal Inferred relationship Some 1
Instability of left elbow joint (finding) Has interpretation True Abnormal Inferred relationship Some 1
A rare, genetic, isolated palmoplantar keratoderma characterized by non-epidermolytic, diffuse hyperkeratotic lesions affecting both the palms and the soles, associated with a tendency of painful fissuring. Contrary to the clinical findings, histologic examination reveals findings suggestive of keratosis palmoplantaris striata, with orthohyperkeratosis featuring widening of the intercellular spaces and disadhesion of keratocytes in the upper epidermal layers. Has interpretation True Abnormal Inferred relationship Some 2
A rare, genetic, ectodermal dysplasia syndrome characterized by persistent skin fragility which manifests with blistering and erosions due to minimal trauma, wooly hair with variable alopecia, hyperkeratotic nail dysplasia, diffuse or focal palmoplantar keratoderma with painful fissuring, and no cardiac abnormalities. Perioral hyperkeratosis may also be associated. Has interpretation True Abnormal Inferred relationship Some 4
A rare, genetic, isolated palmoplantar keratoderma characterized by focal hyperkeratotic lesions affecting the pressure- and mechanical trauma-bearing areas of the palms and soles, as well as hyperkeratotic plaques involving joints, including knees, elbows, ankles and dorsa of interphalangeal joints. Has interpretation True Abnormal Inferred relationship Some 2
Instability of joint of right foot Has interpretation True Abnormal Inferred relationship Some 1
Instability of joint of left knee (finding) Has interpretation True Abnormal Inferred relationship Some 1
Instability of joint of left hand (finding) Has interpretation True Abnormal Inferred relationship Some 1

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