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866053004: Middle interhemispheric variant of holoprosencephaly (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3957071012 Syntelencephaly en Synonym Active Entire term case insensitive SNOMED CT core module
3957072017 Middle interhemispheric variant of holoprosencephaly (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3957073010 Middle interhemispheric variant of holoprosencephaly en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Middle interhemispheric variant of holoprosencephaly Is a Holoprosencephaly sequence true Inferred relationship Existential restriction modifier
Middle interhemispheric variant of holoprosencephaly Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Middle interhemispheric variant of holoprosencephaly Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Middle interhemispheric variant of holoprosencephaly Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Middle interhemispheric variant of holoprosencephaly Is a Congenital anomaly of cerebrum true Inferred relationship Existential restriction modifier
Middle interhemispheric variant of holoprosencephaly Finding site Parietal lobe structure true Inferred relationship Existential restriction modifier 1
Middle interhemispheric variant of holoprosencephaly Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Middle interhemispheric variant of holoprosencephaly Finding site Frontal lobe structure true Inferred relationship Existential restriction modifier 2
Middle interhemispheric variant of holoprosencephaly Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Middle interhemispheric variant of holoprosencephaly Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Middle interhemispheric variant of holoprosencephaly Is a Finding of head region true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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