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449817000: Peters plus syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2012. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2912534012 Peters plus syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2913035014 Peters plus syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
923041000172115 syndrome de Peters plus fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
978641000172119 syndrome d'anomalie de Peters-nanisme fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
873111000172110 peters anomalie met dwerggroei met korte ledematen nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
1002871000172112 syndroom van Peters-plus nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Belgian subset for medical problems in patient health records

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