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204021005: Encephalomyelocele (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
312863016 Encephalomyelocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
589192018 Encephalomyelocele (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
312863016 Encephalomyelocele en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
312863016 Encephalomyelocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
589192018 Encephalomyelocele (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
589192018 Encephalomyelocele (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
589192018 Encephalomyelocele (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
276171000077114 encéphalomyélocèle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
276171000077114 encéphalomyélocèle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained 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 (core metadata concept)
Encephalomyelocele Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept)
Encephalomyelocele Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier (core metadata concept) 3
Encephalomyelocele Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Encephalomyelocele Associated morphology Congenital failure of fusion with herniated tissue false Inferred relationship Existential restriction modifier (core metadata concept) 1
Encephalomyelocele Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Encephalomyelocele Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier (core metadata concept) 1
Encephalomyelocele Associated morphology Congenital protrusion false Inferred relationship Existential restriction modifier (core metadata concept) 2
Encephalomyelocele Is a Disorder of brain false Inferred relationship Existential restriction modifier (core metadata concept)
Encephalomyelocele Associated morphology Congenital failure of fusion with herniated tissue false Inferred relationship Existential restriction modifier (core metadata concept) 1
Encephalomyelocele Finding site Bone structure of cranium true Inferred relationship Existential restriction modifier (core metadata concept) 1
Encephalomyelocele Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Encephalomyelocele Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Encephalomyelocele Finding site Bone structure of head false Inferred relationship Existential restriction modifier (core metadata concept) 2
Encephalomyelocele Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Encephalomyelocele Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Encephalomyelocele Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Encephalomyelocele Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Encephalomyelocele Associated morphology Herniated structure (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Encephalomyelocele Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Encephalomyelocele Associated morphology Developmental failure of fusion (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Encephalomyelocele Is a Congenital anomaly of spinal cord true Inferred relationship Existential restriction modifier (core metadata concept)
Encephalomyelocele Is a Encephalomyelopathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Encephalomyelocele Associated morphology Protrusion true Inferred relationship Existential restriction modifier (core metadata concept) 3
Encephalomyelocele Finding site Spinal cord structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Encephalomyelocele Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Encephalomyelocele Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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