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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
    280471000077112 anomalie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
    561791000077117 anomalie congénitale (anomalie morphologique) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
    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 est un(e) (attribut) structure anormale sur le plan morphologique false Inferred relationship Some
    Congenital anomaly est un(e) (attribut) Developmental abnormality false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Congenital anomaly of jaw morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Congenital blindness morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Congenital macular corneal dystrophy morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Congenital conjunctival cyst morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 2
    Congenital anomaly of optic nerve morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 2
    Congenital anomaly of third eyelid morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 2
    Congenital cartilage anomaly of third eyelid morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 2
    Hypopigmentation of third eyelid morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 2
    Congenital brain damage morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Congenital stenosis of trachea morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Macroencephaly morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Congenital anomaly of cardiovascular system morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Hereditary vascular fragility morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Anencephalus and similar anomalies morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 3
    aplasie du corps calleux morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Congenital atresia of foramen of Magendie morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 3
    Congenital atresia of foramen of Luschka morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Agenesis of eye morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Congenital keratoglobus morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Anterior chamber anomalies morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Corneal size and shape anomalies morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Specified anterior chamber anomalies morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Multiple anterior segment anomalies morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Congenital anomalies of eyelid, lacrimal system and orbit morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Congenital orbit anomalies morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Multiple supernumerary eye muscles morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Hypoplasia of eye muscle morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Ear, face and neck congenital anomalies morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Congenital tricuspid atresia and stenosis morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Tricuspid atresia morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 2
    Congenital insufficiency of aortic valve morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Supernumerary cusps of the mitral valve morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Atresia of cardiac vein morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Vascular ring, aorta morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Anomalous portal vein termination morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Hypoplasia of spinal vessel morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Cerebrovascular system anomalies morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Congenital pharyngeal polyp morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Congenital ectropion of lip morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Renal agenesis and dysgenesis morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Congenital renal atrophy morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Medullary cystic disease, otherwise specified (disorder) morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Renal pelvis and ureter obstructive defects morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Congenital displaced kidney morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    anomalies congénitales de pigmentation de la peau morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Excessive foreskin morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Hydrocephalus with anomaly of aqueduct of Sylvius morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 2
    Congenital malformation of eye, ear and neck morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Congenital malformation of the urinary system morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Pyelon triplex morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Trifid kidney morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Medullary sponge kidney with nephrocalcinosis morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1
    Medullary sponge kidney without nephrocalcinosis morphologie associée (attribut) False Congenital anomaly Inferred relationship Some 1

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    Reference Sets

    Concept inactivation indicator reference set

    Description inactivation indicator reference set

    GB English

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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