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449817000: Peters plus syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2012. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2912534012 Peters plus syndrome en Synonym Active Case sensitive SNOMED CT core
2913035014 Peters plus syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Peters plus syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Peters plus syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Peters plus syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Peters plus syndrome Associated morphology Congenital anomaly false Inferred relationship Some 2
Peters plus syndrome Is a Hereditary disorder of the visual system true Inferred relationship Some
Peters plus syndrome Is a Congenital anomaly of anterior chamber of eye true Inferred relationship Some
Peters plus syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Peters plus syndrome Occurrence Congenital false Inferred relationship Some
Peters plus syndrome Finding site Anterior chamber of eye structure false Inferred relationship Some 2
Peters plus syndrome Occurrence Congenital true Inferred relationship Some 1
Peters plus syndrome Associated morphology Developmental abnormality false Inferred relationship Some 1
Peters plus syndrome Finding site Anterior chamber of eye structure true Inferred relationship Some 1

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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