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2107001: Anisomelia (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4647012 Anisomelia en Synonym Active Case insensitive SNOMED CT core
750324019 Anisomelia (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anisomelia Pathological process Pathological developmental process true Inferred relationship Some 1
Anisomelia Is a Congenital anomaly of limb true Inferred relationship Some
Anisomelia Finding site Limb structure false Inferred relationship Some 3
Anisomelia Associated morphology Congenital growth disproportion false Inferred relationship Some 3
Anisomelia Occurrence Congenital false Inferred relationship Some 3
Anisomelia Associated morphology Developmental abnormality false Inferred relationship Some 2
Anisomelia Finding site Limb structure false Inferred relationship Some 2
Anisomelia Associated morphology Congenital growth disproportion true Inferred relationship Some 1
Anisomelia Occurrence Congenital true Inferred relationship Some 1
Anisomelia Finding site Limb structure true Inferred relationship Some 1
Anisomelia Occurrence Congenital false Inferred relationship Some
Anisomelia Associated morphology Congenital growth disproportion false Inferred relationship Some 1
Anisomelia Finding site Musculoskeletal structure of limb false Inferred relationship Some
Anisomelia Associated morphology Developmental abnormality false Inferred relationship Some
Anisomelia Finding site Limb structure false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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