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176574003: Agenesis of both forepaws and both hindpaws (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2015. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    273374011 Agenesis of both forepaws and both hindpaws en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    559261017 Agenesis of both forepaws and both hindpaws (disorder) 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
    Agenesis of both forepaws and both hindpaws Is a Congenital complete absence of limb false Inferred relationship Some
    Agenesis of both forepaws and both hindpaws Associated morphology anomalie du développement false Inferred relationship Some
    Agenesis of both forepaws and both hindpaws Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 1
    Agenesis of both forepaws and both hindpaws Occurrence Congenital false Inferred relationship Some
    Agenesis of both forepaws and both hindpaws Finding site Limb structure false Inferred relationship Some 1
    Agenesis of both forepaws and both hindpaws Finding site Musculoskeletal structure of limb false Inferred relationship Some
    Agenesis of both forepaws and both hindpaws Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 1
    Agenesis of both forepaws and both hindpaws Finding site Limb structure false Inferred relationship Some 1
    Agenesis of both forepaws and both hindpaws Occurrence Congenital false Inferred relationship Some 2
    Agenesis of both forepaws and both hindpaws Finding site Limb structure false Inferred relationship Some 2
    Agenesis of both forepaws and both hindpaws Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    MOVED TO association reference set

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