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89434002: Complete aphalangia of lower limb (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module Reference Sets
148278016 Complete aphalangia of lower limb en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
832327010 Complete aphalangia of lower limb (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)

0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Complete aphalangia of lower limb Is a Congenital absence of all toes false Inferred relationship Some
Complete aphalangia of lower limb Is a Congenital abnormality of foot and toes (disorder) false Inferred relationship Some
Complete aphalangia of lower limb Occurrence Congenital false Inferred relationship Some
Complete aphalangia of lower limb Associated morphology Developmental anomaly false Inferred relationship Some
Complete aphalangia of lower limb Finding site Connective tissue false Inferred relationship Some
Complete aphalangia of lower limb Finding site Musculoskeletal structure of foot (body structure) false Inferred relationship Some 1
Complete aphalangia of lower limb Is a Congenital absence of foot (disorder) false Inferred relationship Some
Complete aphalangia of lower limb Finding site Structure of all toes false Inferred relationship Some 1
Complete aphalangia of lower limb Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 1
Complete aphalangia of lower limb Associated morphology Congenital anomaly false Inferred relationship Some 1
Complete aphalangia of lower limb Is a Congenital malformation false Inferred relationship Some
Complete aphalangia of lower limb Is a Congenital absence of toe true Inferred relationship Some
Complete aphalangia of lower limb Is a Congenital absence of skeletal bone true Inferred relationship Some
Complete aphalangia of lower limb Finding site Structure of phalanx of toe (body structure) false Inferred relationship Some 1
Complete aphalangia of lower limb Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 1
Complete aphalangia of lower limb Finding site Structure of phalanx of toe (body structure) false Inferred relationship Some 1
Complete aphalangia of lower limb Occurrence Congenital false Inferred relationship Some 2
Complete aphalangia of lower limb Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 2
Complete aphalangia of lower limb Finding site Structure of phalanx of toe (body structure) false Inferred relationship Some 2
Complete aphalangia of lower limb Occurrence Congenital true Inferred relationship Some 1
Complete aphalangia of lower limb Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 1
Complete aphalangia of lower limb Finding site Entire toe (body structure) false Inferred relationship Some 1
Complete aphalangia of lower limb Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Complete aphalangia of lower limb Is a Adactyly false Inferred relationship Some
Complete aphalangia of lower limb Is a Finding of musculoskeletal structure of toe true Inferred relationship Some
Complete aphalangia of lower limb Finding site Entire phalanx of toe true Inferred relationship Some 1
Complete aphalangia of lower limb Is a Finding of bone of lower limb (finding) true Inferred relationship Some
Complete aphalangia of lower limb Associated morphology Absence (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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