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107656002: Congenital anomaly (morphologic abnormality)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    172092016 Congenital anomaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    593259012 Congenital anomaly (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital anomaly Is a Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some
    Congenital anomaly Is a Developmental anomaly false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Congenital arteriovenous malformation of gastrointestinal tract (disorder) Associated morphology False Congenital anomaly Inferred relationship Some 2
    Congenital vesico-ureteric reflux Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital sclerocornea Associated morphology False Congenital anomaly Inferred relationship Some 1
    Anterior lentiglobus Associated morphology False Congenital anomaly Inferred relationship Some 1
    Posterior lenticonus Associated morphology False Congenital anomaly Inferred relationship Some 1
    Posterior lentiglobus Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital anomaly of choroid Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital hypoplasia of choroid Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital hypopigmentation of choroid Associated morphology False Congenital anomaly Inferred relationship Some 1
    Retinal dysplasia Associated morphology False Congenital anomaly Inferred relationship Some 1
    Multifocal retinal dysplasia Associated morphology False Congenital anomaly Inferred relationship Some 1
    Geographic retinal dysplasia Associated morphology False Congenital anomaly Inferred relationship Some 1
    Diffuse retinal dysplasia Associated morphology False Congenital anomaly Inferred relationship Some 1
    Hypoplasia of the optic nerve Associated morphology False Congenital anomaly Inferred relationship Some 3
    Hypoplasia of the optic nerve Associated morphology False Congenital anomaly Inferred relationship Some 2
    Macropalpebral fissure Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital displacement of punctum lacrimale Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital anomaly of third eyelid Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital cartilage anomaly of third eyelid Associated morphology False Congenital anomaly Inferred relationship Some 2
    Hypopigmentation of third eyelid Associated morphology False Congenital anomaly Inferred relationship Some 1
    Hypoplasia of iris Associated morphology False Congenital anomaly Inferred relationship Some 2
    Congenital syphilitic choroiditis Associated morphology False Congenital anomaly Inferred relationship Some 2
    Supramitral left atrial ring Associated morphology False Congenital anomaly Inferred relationship Some 1
    Tricuspid leaflet dysplasia Associated morphology False Congenital anomaly Inferred relationship Some 1
    Tricuspid annulus hypoplasia Associated morphology False Congenital anomaly Inferred relationship Some 2
    Dilatation of tricuspid annulus (disorder) Associated morphology False Congenital anomaly Inferred relationship Some 2
    Overriding tricuspid valve Associated morphology False Congenital anomaly Inferred relationship Some 1
    Straddling tricuspid valve Associated morphology False Congenital anomaly Inferred relationship Some 1
    Tricuspid leaflet abnormality Associated morphology False Congenital anomaly Inferred relationship Some 1
    Absent tricuspid leaflet Associated morphology False Congenital anomaly Inferred relationship Some 2
    Tricuspid valve prolapse Associated morphology False Congenital anomaly Inferred relationship Some 2
    Mitral valve dysplasia Associated morphology False Congenital anomaly Inferred relationship Some 1
    Mitral leaflet dysplasia Associated morphology False Congenital anomaly Inferred relationship Some 1
    Overriding mitral valve Associated morphology False Congenital anomaly Inferred relationship Some 1
    Dilation of mitral annulus (disorder) Associated morphology False Congenital anomaly Inferred relationship Some 1
    Straddling mitral valve Associated morphology False Congenital anomaly Inferred relationship Some 1
    Ebstein-like downward displacement of mitral valve Associated morphology False Congenital anomaly Inferred relationship Some 2
    Anterior leaflet of mitral valve attached to septum Associated morphology False Congenital anomaly Inferred relationship Some 1
    Accessory tissue on mitral leaflet Associated morphology False Congenital anomaly Inferred relationship Some 1
    Mitral papillary muscle abnormality Associated morphology False Congenital anomaly Inferred relationship Some 1
    Fused mitral papillary muscles Associated morphology False Congenital anomaly Inferred relationship Some 1
    Hypoplastic mitral papillary muscle Associated morphology False Congenital anomaly Inferred relationship Some 1
    Pulmonary valve cusp hypoplasia Associated morphology False Congenital anomaly Inferred relationship Some 1
    Pulmonary valve ring hypoplasia Associated morphology False Congenital anomaly Inferred relationship Some 1
    Commissural fusion of aortic valve Associated morphology False Congenital anomaly Inferred relationship Some 1
    Eccentric opening of aortic valve Associated morphology False Congenital anomaly Inferred relationship Some 2
    Aortic valve dysplasia (disorder) Associated morphology False Congenital anomaly Inferred relationship Some 1
    Aortic valve cusp abnormality Associated morphology False Congenital anomaly Inferred relationship Some 2
    Aortic valve cusp prolapse Associated morphology False Congenital anomaly Inferred relationship Some 1
    Vascular rings Associated morphology False Congenital anomaly Inferred relationship Some 1
    Lobulated tongue Associated morphology False Congenital anomaly Inferred relationship Some 4
    Hamartoma of tongue Associated morphology False Congenital anomaly Inferred relationship Some 1
    Tracheobiliary fistula Associated morphology False Congenital anomaly Inferred relationship Some 1
    Familial hypoplastic, glomerulocystic kidney Associated morphology False Congenital anomaly Inferred relationship Some 2
    Cake kidney Associated morphology False Congenital anomaly Inferred relationship Some 1
    Bifid kidney Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital calyceal diverticulum Associated morphology False Congenital anomaly Inferred relationship Some 1
    Nephronophthisis - medullary cystic disease (disorder) Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital obstructive defect of renal pelvis Associated morphology False Congenital anomaly Inferred relationship Some 1
    Megacystis-megaureter syndrome Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital gastrointestinal-urinary tract fistula Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital postural curvature of spine Associated morphology False Congenital anomaly Inferred relationship Some 1
    Bregeat's syndrome Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital valvular insufficiency Associated morphology False Congenital anomaly Inferred relationship Some 1
    Persistent vertical vein Associated morphology False Congenital anomaly Inferred relationship Some 1
    Aland eye disease and ocular albinism Associated morphology False Congenital anomaly Inferred relationship Some 1
    Bilateral renal hypoplasia Associated morphology False Congenital anomaly Inferred relationship Some 1
    Fibrocystic kidney disease Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital renal failure Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital abnormality of thoracic aorta and pulmonary arteries Associated morphology False Congenital anomaly Inferred relationship Some 1
    Transient tricuspid regurgitation of newborn Associated morphology False Congenital anomaly Inferred relationship Some 2
    Congenital nephritis Associated morphology False Congenital anomaly Inferred relationship Some 2
    Congenital uraemia Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital hydrocalicosis Associated morphology False Congenital anomaly Inferred relationship Some 1
    Venous remnant Associated morphology False Congenital anomaly Inferred relationship Some 1
    Persistent descending vein Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital abnormality of vein Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital anomaly of the urinary tract proper (disorder) Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital agenesis of brainstem nuclei Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital nystagmus with sensory abnormality Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital nystagmus without sensory abnormality Associated morphology False Congenital anomaly Inferred relationship Some 1
    Persistent hyperplastic primary vitreous Associated morphology False Congenital anomaly Inferred relationship Some 2
    Gingival cysts of infant Associated morphology False Congenital anomaly Inferred relationship Some 3
    Mesio-occlusion of teeth Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital anteversion of femur Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital portal-systemic shunt Associated morphology False Congenital anomaly Inferred relationship Some 1
    Duane's syndrome, type 1 Associated morphology False Congenital anomaly Inferred relationship Some 1
    Duane's syndrome, type 2 Associated morphology False Congenital anomaly Inferred relationship Some 1
    Duane's syndrome, type 3 Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital anomaly of mandible Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital anomaly of ocular adnexa (disorder) Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital structural abnormality of cornea Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital anomaly of lens (disorder) Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital corneal opacity interfering with vision Associated morphology False Congenital anomaly Inferred relationship Some 1
    Incomplete anencephaly Associated morphology False Congenital anomaly Inferred relationship Some 3
    Congenital anomaly of aortic valve Associated morphology False Congenital anomaly Inferred relationship Some 1
    Embedded tooth Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital anomaly of trachea Associated morphology False Congenital anomaly Inferred relationship Some 1
    Congenital phlebectasia Associated morphology False Congenital anomaly Inferred relationship Some 2
    Atrophia bulborum hereditaria Associated morphology False Congenital anomaly Inferred relationship Some 1
    Double kidney AND/OR pelvis Associated morphology False Congenital anomaly Inferred relationship Some 2

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    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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