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866053004: Middle interhemispheric variant of holoprosencephaly (disorder)


Status: current, Primitive. Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

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


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 Some
Middle interhemispheric variant of holoprosencephaly Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Middle interhemispheric variant of holoprosencephaly Occurrence Congenital true Inferred relationship Some 1
Middle interhemispheric variant of holoprosencephaly Pathological process Pathological developmental process true Inferred relationship Some 1
Middle interhemispheric variant of holoprosencephaly Is a Congenital anomaly of cerebrum true Inferred relationship Some
Middle interhemispheric variant of holoprosencephaly Finding site Parietal lobe structure true Inferred relationship Some 1
Middle interhemispheric variant of holoprosencephaly Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Middle interhemispheric variant of holoprosencephaly Finding site Frontal lobe structure true Inferred relationship Some 2
Middle interhemispheric variant of holoprosencephaly Occurrence Congenital true Inferred relationship Some 2
Middle interhemispheric variant of holoprosencephaly Pathological process Pathological developmental process true Inferred relationship Some 2
Middle interhemispheric variant of holoprosencephaly Is a Finding of head region true 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

Description inactivation indicator reference set

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