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243996003: Entire limb (body structure)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
364884010 Entire limb en Synonym Active Entire term case insensitive SNOMED CT core module
633759011 Entire limb (body structure) en Fully specified name Active Entire term case insensitive SNOMED CT core module


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Entire limb Is a Limb structure true Inferred relationship Existential restriction modifier
Entire limb Is a Entire body part false Inferred relationship Existential restriction modifier
Entire limb Part of Entire body as a whole false Additional relationship Existential restriction modifier
Entire limb Laterality Side true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Short rib polydactyly syndrome type I Finding site True Entire limb Inferred relationship Existential restriction modifier 2
Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome Finding site True Entire limb Inferred relationship Existential restriction modifier 1
Radial deficiency, tibial hypoplasia syndrome Finding site True Entire limb Inferred relationship Existential restriction modifier 2
Diastrophic dysplasia Finding site True Entire limb Inferred relationship Existential restriction modifier 2
Macromelia Finding site True Entire limb Inferred relationship Existential restriction modifier 1
Micromelic dwarfism Fryn type Finding site True Entire limb Inferred relationship Existential restriction modifier 1
Longitudinal deficiency of limb Finding site True Entire limb Inferred relationship Existential restriction modifier 1
Dysraphism, cleft lip and palate, limb reduction defect syndrome Finding site True Entire limb Inferred relationship Existential restriction modifier 3
Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome Finding site True Entire limb Inferred relationship Existential restriction modifier 2
Femur fibula ulna complex Finding site True Entire limb Inferred relationship Existential restriction modifier 3

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