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6920004: Defect (morphologic abnormality)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2023. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    12439018 Defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    809119010 Defect (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2610311000005115 Defekt da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Defekt Is a Mechanical abnormality false Inferred relationship Some
    Defekt Is a Mechanical lesion false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Peripheral visual field defect of right eye (finding) Associated morphology False Defekt Inferred relationship Some 1
    Pentalogy of Fallot Associated morphology False Defekt Inferred relationship Some 1
    Congenital pericardial defect (disorder) Associated morphology False Defekt Inferred relationship Some 1
    Fetal abdominal wall defect (disorder) Associated morphology False Defekt Inferred relationship Some 1
    Transposition of great arteries with concordant atrioventricular connections and ventricular septal defect Associated morphology False Defekt Inferred relationship Some 3
    Transposition of great arteries with concordant atrioventricular connections and ventricular septal defect and left ventricular outflow tract obstruction Associated morphology False Defekt Inferred relationship Some 3
    Double outlet right ventricle with subaortic ventricular septal defect and pulmonary stenosis Fallot type (disorder) Associated morphology False Defekt Inferred relationship Some 3
    Corneal epithelial defect following penetrating keratoplasty Associated morphology False Defekt Inferred relationship Some 2
    Bilateral full thickness hole of macula of eyes Associated morphology False Defekt Inferred relationship Some 1
    Bilateral full thickness hole of macula of eyes Associated morphology False Defekt Inferred relationship Some 2
    Residual ventricular septal defect following procedure (disorder) Associated morphology False Defekt Inferred relationship Some 1
    Recurrent ventricular septal defect following procedure (disorder) Associated morphology False Defekt Inferred relationship Some 1
    Onycho-tricho-dysplasia neutropenia syndrome Associated morphology False Defekt Inferred relationship Some 2
    Sabinas brittle hair syndrome (disorder) Associated morphology False Defekt Inferred relationship Some 2
    Spondylolysis of thoracic vertebra (disorder) Associated morphology False Defekt Inferred relationship Some 1
    Rhegmatogenous retinal detachment with multiple breaks (disorder) Associated morphology False Defekt Inferred relationship Some 2
    Ny partiel nethindeløsning med multiple defekter Associated morphology False Defekt Inferred relationship Some 2
    Repair of supracristal defect with tissue graft Direct morphology False Defekt Inferred relationship Some 2
    Closure of defect of atrioventricular septum using tissue graft Direct morphology False Defekt Inferred relationship Some 1
    Repair of ventricular septal defect with tissue graft Direct morphology False Defekt Inferred relationship Some 1
    Stafne idiopathic bone cavity of mandible Associated morphology False Defekt Inferred relationship Some 1
    Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome is a rare, genetic, non-dystrophic congenital myopathy disorder characterized by a neonatal-onset of severe generalized hypotonia associated with mild psychomotor delay, congenital strabismus with abducens nerve palsy, and atrial and/or ventricular septal defects. Cryptorchidism is commonly reported in male patients and muscle biopsy typically reveals increased variability in muscle fiber size. Associated morphology False Defekt Inferred relationship Some 3
    Corneal epithelial defect Associated morphology False Defekt Inferred relationship Some 1
    Persistent corneal epithelial defect Associated morphology False Defekt Inferred relationship Some 1
    Reconstruction of cranial defect with free flap Direct morphology False Defekt Inferred relationship Some 1
    Reconstruction of defect of nasal sinus with local flap Direct morphology False Defekt Inferred relationship Some 1
    Repair of defect of palate with skin flap Direct morphology False Defekt Inferred relationship Some 1
    Reconstruction of defect of nasal sinus with microvascular transferred flap Direct morphology False Defekt Inferred relationship Some 1
    Retinal nerve fiber bundle defect of left eye Associated morphology False Defekt Inferred relationship Some 1
    Defect of nerve fiber layer of right retina (disorder) Associated morphology False Defekt Inferred relationship Some 1
    Bilateral defect of nerve fibre layer of retinas Associated morphology False Defekt Inferred relationship Some 1
    Bilateral defect of nerve fibre layer of retinas Associated morphology False Defekt Inferred relationship Some 2
    Closure of atrial septal defect using robotic assistance (procedure) Direct morphology False Defekt Inferred relationship Some 1
    Acquired atrioventricular septal defect Associated morphology False Defekt Inferred relationship Some 1
    Primary ciliary dyskinesia - retinitis pigmentosa is an X-linked ciliary dysfunction of both respiratory epithelium and photoreceptors of the retina leading to ocular disorders (mild night blindness, constriction of the visual field, and scotopic and photopic ERG responses reduced to 30-60%) associated with primary ciliary dyskinesia manifestations (chronic bronchorrhea with bronchiectasis and chronic sinusitis) and sensorineural hearing loss. Associated morphology False Defekt Inferred relationship Some 2
    Break of retina with schisis of retina (disorder) Associated morphology False Defekt Inferred relationship Some 3
    Multiple breaks of retina with schisis of retina (disorder) Associated morphology False Defekt Inferred relationship Some 3
    Spondylolytic spondylolisthesis Associated morphology False Defekt Inferred relationship Some 1
    Defect in vaginal wall (finding) Associated morphology False Defekt Inferred relationship Some 1

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    Reference Sets

    Concept inactivation indicator reference set

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    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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