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733606001: Summitt syndrome (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    3499668012 Summitt syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3499669016 Summitt syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3499670015 Summitt's acrocephalosyndactyly en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3500047010 Summitt syndrome is an extremely rare disorder originally described in two brothers and with characteristics of mild to severe craniosynostosis and syndactyly, obesity and normal intelligence. Acrocephaly, brachydactyly, clinodactyly, mild syndactyly of the hands and feet, genu valgum and marked obesity were later described in another patient. There have been no further descriptions in the literature since 1979. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3499668012 Summitt syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3499669016 Summitt syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3499670015 Summitt's acrocephalosyndactyly en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3500047010 Summitt syndrome is an extremely rare disorder originally described in two brothers and with characteristics of mild to severe craniosynostosis and syndactyly, obesity and normal intelligence. Acrocephaly, brachydactyly, clinodactyly, mild syndactyly of the hands and feet, genu valgum and marked obesity were later described in another patient. There have been no further descriptions in the literature since 1979. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3384811001000119 Summitt-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    967431000172117 syndrome de Summitt fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    967431000172117 syndrome de Summitt fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    3384811001000119 Summitt-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    syndrome de Summitt Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Summitt Is a Acrocephalosyndactyly false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Summitt Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Summitt Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Summitt Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Summitt Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome de Summitt Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
    syndrome de Summitt Associated morphology Congenital premature fusion false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome de Summitt Finding site Joint structure of suture of skull false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome de Summitt Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier (core metadata concept) 4
    syndrome de Summitt Finding site Digit structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
    syndrome de Summitt Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome de Summitt Finding site Joint structure of suture of skull false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Summitt Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Summitt Associated morphology Congenital premature fusion false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Summitt Finding site Digit structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome de Summitt Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Summitt Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome de Summitt Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome de Summitt Is a Developmental hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Summitt Associated morphology Premature fusion (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Summitt Associated morphology Abnormally fused structure (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    GB English

    US English

    REPLACED BY association reference set (foundation metadata concept)

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