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204021005: Encephalomyelocele (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
312863016 Encephalomyelocele en Synonym Active Entire term case insensitive SNOMED CT core module
589192018 Encephalomyelocele (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Encephalomyelocele Is a Encephalocele true Inferred relationship Existential restriction modifier
Encephalomyelocele Finding site Brain structure false Inferred relationship Existential restriction modifier
Encephalomyelocele Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier 3
Encephalomyelocele Occurrence Congenital false Inferred relationship Existential restriction modifier
Encephalomyelocele Associated morphology Congenital failure of fusion with herniated tissue false Inferred relationship Existential restriction modifier 1
Encephalomyelocele Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Encephalomyelocele Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier 1
Encephalomyelocele Associated morphology Congenital protrusion false Inferred relationship Existential restriction modifier 2
Encephalomyelocele Is a Disorder of brain false Inferred relationship Existential restriction modifier
Encephalomyelocele Associated morphology Congenital failure of fusion with herniated tissue false Inferred relationship Existential restriction modifier 1
Encephalomyelocele Finding site Bone structure of cranium true Inferred relationship Existential restriction modifier 1
Encephalomyelocele Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Encephalomyelocele Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Encephalomyelocele Finding site Bone structure of head false Inferred relationship Existential restriction modifier 2
Encephalomyelocele Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Encephalomyelocele Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Encephalomyelocele Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Encephalomyelocele Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 2
Encephalomyelocele Associated morphology Herniated structure true Inferred relationship Existential restriction modifier 2
Encephalomyelocele Finding site Brain structure true Inferred relationship Existential restriction modifier 2
Encephalomyelocele Associated morphology Developmental failure of fusion true Inferred relationship Existential restriction modifier 1
Encephalomyelocele Is a Congenital anomaly of spinal cord true Inferred relationship Existential restriction modifier
Encephalomyelocele Is a Encephalomyelopathy true Inferred relationship Existential restriction modifier
Encephalomyelocele Associated morphology Protrusion true Inferred relationship Existential restriction modifier 3
Encephalomyelocele Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 3
Encephalomyelocele Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Encephalomyelocele Occurrence Congenital true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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