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699420006: Hemifacial myohyperplasia (disorder)


Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2984137015 Hemifacial myohyperplasia en Synonym Active Case insensitive SNOMED CT core
2984279017 Hemifacial myohyperplasia (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
Hemifacial myohyperplasia Pathological process Pathological developmental process true Inferred relationship Some 1
Hemifacial myohyperplasia Associated morphology Deformity true Inferred relationship Some 1
Hemifacial myohyperplasia Is a Congenital deformity of face true Inferred relationship Some
Hemifacial myohyperplasia Occurrence Congenital false Inferred relationship Some
Hemifacial myohyperplasia Associated morphology Congenital deformity false Inferred relationship Some 2
Hemifacial myohyperplasia Finding site Face structure false Inferred relationship Some 2
Hemifacial myohyperplasia Occurrence Congenital true Inferred relationship Some 1
Hemifacial myohyperplasia Finding site Face structure true Inferred relationship Some 1
Hemifacial myohyperplasia Associated morphology Congenital deformity 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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