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61295008: Congenital abnormal number (morphologic abnormality)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2024. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    101850015 Congenital abnormal number en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    800341012 Congenital abnormal number (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 abnormal number Is a Congenital growth alteration false Inferred relationship Some
    Congenital abnormal number Is a Growth alteration false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Hypodontia and nail dysgenesis Associated morphology False Congenital abnormal number Inferred relationship Some 6
    Unicommissural unicuspid aortic valve (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Anterior-posterior orientation of bicuspid pulmonary valve (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Acommissural unicuspid pulmonary valve (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Abnormal number of pulmonary valve cusps Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Unicommissural unicuspid pulmonary valve (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Right-left orientation of bicuspid aortic valve (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Unicuspid aortic valve (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Bicuspid doming of aortic cusp Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Unicuspid pulmonary valve (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Monocuspid cardiac valve Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Bicuspid pulmonary valve Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Abnormal number of leaflets Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Abnormal number of cardiac valve cusps (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Acommissural unicuspid aortic valve (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Bicuspid aortic valve Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Bicuspid cardiac valve Associated morphology False Congenital abnormal number Inferred relationship Some 3
    Quadricuspid aortic valve Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Quadricuspid pulmonary valve Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Right-left orientation of bicuspid pulmonary valve (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Anterior-posterior orientation of bicuspid aortic valve (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Abnormal number of aortic valve cusps Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Additional sex chromosome Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Multiple renal arteries Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Congenital hypodontia, multiple teeth, related to systemic disease Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Familial hypodontia Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Hypodontia and nail dysgenesis Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Partial congenital absence of teeth Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Familial hypodontia Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Hypodontia and nail dysgenesis Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Congenital hypodontia, multiple teeth, unrelated to systemic disease Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Congenital hypodontia, multiple teeth, related to systemic disease Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Congenital hypodontia, multiple teeth, unrelated to systemic disease Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Bicuspid cardiac valve Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Deafness and oligodontia syndrome (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 3
    Cleft palate with stapes fixation and oligodontia syndrome (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 5
    Taurodontia with absent teeth and sparse hair syndrome (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 6
    Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 5
    Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 7
    Odontoleukodystrophy (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Steroid dehydrogenase deficiency and dental anomaly syndrome (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Familial bicuspid aortic valve (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Pseudounicornuate uterus (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Taurodontia with absent teeth and sparse hair syndrome (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Deafness and oligodontia syndrome (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Oligomeganephronic hypoplasia of kidney Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Anodontia of permanent dentition Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Complete congenital absence of teeth Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Cleft palate with stapes fixation and oligodontia syndrome (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 3
    Spondyloepimetaphyseal dysplasia, abnormal dentition syndrome (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 3
    Oligodontia and cancer predisposition syndrome Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Congenital abnormal number of coronary ostia Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Oligodontia Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Single coronary artery dividing into right coronary artery and left coronary artery (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Single left coronary artery supplying all of heart with usual distribution of right coronary artery derived from distal left coronary artery (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Single right coronary artery supplying all of heart with usual distribution of left coronary artery derived from distal right coronary artery (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 1
    Epidermolysis bullosa simplex with hypodontia (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Bicuspid aortic valve-associated aortopathy (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    X-linked hypodontia (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    X-linked oligodontia (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Taurodontia with absent teeth and sparse hair syndrome (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 4
    Oligodontia and cancer predisposition syndrome Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Cleft palate with stapes fixation and oligodontia syndrome (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Congenital absence of one tooth Associated morphology False Congenital abnormal number Inferred relationship Some 2
    Trichodermodysplasia and dental alterations syndrome Associated morphology False Congenital abnormal number Inferred relationship Some 5
    Ectodermal dysplasia trichoodontoonychial type (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 5
    Four vessels in umbilical cord (disorder) Associated morphology False Congenital abnormal number Inferred relationship Some 1

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    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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