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239018005: Schoepf-Schulz-Passage syndrome (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-May 2025. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    358197018 Schoepf-Schulz-Passage syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    627977017 Schoepf-Schulz-Passage syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    5026611000241115 syndrome de Schoef-Schulz-Passage fr Synonym (core metadata concept) Active Only initial character case insensitive (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 Schoef-Schulz-Passage Is a Ectodermal dysplasia with hair-tooth-nail defects (disorder) false Inferred relationship Some
    syndrome de Schoef-Schulz-Passage Associated morphology Dysplasia false Inferred relationship Some 1
    syndrome de Schoef-Schulz-Passage Finding site Skin structure false Inferred relationship Some 1
    syndrome de Schoef-Schulz-Passage Occurrence Congenital false Inferred relationship Some
    syndrome de Schoef-Schulz-Passage Associated morphology anomalie congénitale false Inferred relationship Some
    syndrome de Schoef-Schulz-Passage Associated morphology Congenital dysplasia false Inferred relationship Some 1
    syndrome de Schoef-Schulz-Passage Associated morphology Congenital dysplasia false Inferred relationship Some 1
    syndrome de Schoef-Schulz-Passage Finding site Skin structure false Inferred relationship Some 1
    syndrome de Schoef-Schulz-Passage Finding site Skin structure false Inferred relationship Some 2
    syndrome de Schoef-Schulz-Passage Occurrence Congenital false Inferred relationship Some 2
    syndrome de Schoef-Schulz-Passage Associated morphology anomalie du développement false Inferred relationship Some 2
    syndrome de Schoef-Schulz-Passage Occurrence Congenital false Inferred relationship Some 3
    syndrome de Schoef-Schulz-Passage Associated morphology Congenital dysplasia false Inferred relationship Some 3
    syndrome de Schoef-Schulz-Passage Finding site Ectoderm structure false Inferred relationship Some 3
    syndrome de Schoef-Schulz-Passage Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    syndrome de Schoef-Schulz-Passage Occurrence Congenital false Inferred relationship Some 1
    syndrome de Schoef-Schulz-Passage Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
    syndrome de Schoef-Schulz-Passage Finding site Ectoderm structure false Inferred relationship Some 1
    syndrome de Schoef-Schulz-Passage Associated morphology Morphologically abnormal structure false Inferred relationship Some 2
    syndrome de Schoef-Schulz-Passage Associated morphology Morphologically abnormal structure false Inferred relationship Some 3
    syndrome de Schoef-Schulz-Passage Associated morphology Morphologically abnormal structure false Inferred relationship Some 4
    syndrome de Schoef-Schulz-Passage Finding site Hair structure (body structure) false Inferred relationship Some 4
    syndrome de Schoef-Schulz-Passage Occurrence Congenital false Inferred relationship Some 4
    syndrome de Schoef-Schulz-Passage Finding site Nail unit is a complex structure which consists of nail plate, nail bed, nail root and skin around the nail plate. false Inferred relationship Some 2
    syndrome de Schoef-Schulz-Passage Finding site Tooth structure false Inferred relationship Some 3
    syndrome de Schoef-Schulz-Passage Pathological process (attribute) Pathological developmental process false Inferred relationship Some 4
    syndrome de Schoef-Schulz-Passage Pathological process (attribute) Pathological developmental process false Inferred relationship Some 3

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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