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19109004: Syringomyelobulbia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
32207016 Syringomyelobulbia en Synonym Active Case insensitive SNOMED CT core
746893013 Syringomyelobulbia (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
Syringomyelobulbia Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Syringomyelobulbia Occurrence Congenital true Inferred relationship Some 1
Syringomyelobulbia Pathological process Pathological developmental process true Inferred relationship Some 1
Syringomyelobulbia Is a Congenital anomaly of trunk false Inferred relationship Some
Syringomyelobulbia Is a Congenital anomaly of nervous system false Inferred relationship Some
Syringomyelobulbia Is a Spinal cord disease false Inferred relationship Some
Syringomyelobulbia Associated morphology Congenital anomaly false Inferred relationship Some 1
Syringomyelobulbia Finding site Structure of nervous system false Inferred relationship Some 1
Syringomyelobulbia Is a Congenital anomaly of spinal cord true Inferred relationship Some
Syringomyelobulbia Finding site Spinal cord structure true Inferred relationship Some 1
Syringomyelobulbia Associated morphology Congenital anomaly false Inferred relationship Some 1
Syringomyelobulbia Is a Congenital anomaly of nervous system false Inferred relationship Some
Syringomyelobulbia Is a Spinal cord disease false Inferred relationship Some
Syringomyelobulbia Occurrence Congenital false Inferred relationship Some 2
Syringomyelobulbia Associated morphology Developmental abnormality false Inferred relationship Some 2
Syringomyelobulbia Finding site Structure of nervous system false Inferred relationship Some 2
Syringomyelobulbia Finding site Spinal cord structure false Inferred relationship Some 1
Syringomyelobulbia Occurrence Congenital false Inferred relationship Some

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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