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314270008: Persistent hyperplastic primary vitreous (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
458602016 Persistent hyperplastic primary vitreous en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
711059016 Persistent hyperplastic primary vitreous (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5244221012 PHPV - persistent hyperplastic primary vitreous en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5244222017 Persistent foetal vasculature syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5244223010 Persistent fetal vasculature syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
458602016 Persistent hyperplastic primary vitreous en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
458602016 Persistent hyperplastic primary vitreous en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
711059016 Persistent hyperplastic primary vitreous (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
711059016 Persistent hyperplastic primary vitreous (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2579339018 PHPV - Persistent hyperplastic primary vitreous en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5244221012 PHPV - persistent hyperplastic primary vitreous en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5244222017 Persistent foetal vasculature syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5244223010 Persistent fetal vasculature syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3429011001000111 Persistierender hyperplastischer primärer Vitreus de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
974591000172119 cécité congénitale par défaut d'attachement de la rétine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
987911000172116 persistance du vitré primitif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
974591000172119 cécité congénitale par défaut d'attachement de la rétine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
987911000172116 persistance du vitré primitif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3429011001000111 Persistierender hyperplastischer primärer Vitreus de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Persistent hyperplastic primary vitreous Is a Persistent primary vitreous false Inferred relationship Existential restriction modifier (core metadata concept)
Persistent hyperplastic primary vitreous Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Persistent hyperplastic primary vitreous Finding site Posterior eyeball segment structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Persistent hyperplastic primary vitreous Associated morphology Persistent embryonic structure (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Persistent hyperplastic primary vitreous Finding site Vitreous body structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Persistent hyperplastic primary vitreous Finding site Structure of primary vitreous true Inferred relationship Existential restriction modifier (core metadata concept) 1
Persistent hyperplastic primary vitreous Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Persistent hyperplastic primary vitreous Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Persistent hyperplastic primary vitreous Finding site Structure of primary vitreous false Inferred relationship Existential restriction modifier (core metadata concept) 1
Persistent hyperplastic primary vitreous Finding site Vitreous body structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Persistent hyperplastic primary vitreous Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Persistent hyperplastic primary vitreous Associated morphology Persistent embryonic structure (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Persistent hyperplastic primary vitreous Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Persistent hyperplastic primary vitreous Associated morphology Persistent embryonic structure (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Persistent hyperplastic primary vitreous Finding site Structure of primary vitreous false Inferred relationship Existential restriction modifier (core metadata concept) 3
Persistent hyperplastic primary vitreous Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Persistent hyperplastic primary vitreous Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Persistent hyperplastic primary vitreous Is a Embryological remnant true Inferred relationship Existential restriction modifier (core metadata concept)
Persistent hyperplastic primary vitreous Is a Disorder of embryonic structure (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Oculopalatocerebral syndrome is characterized by the association of four anomalies: intellectual deficit, microcephaly, palate anomalies and ocular abnormalities. Is a True Persistent hyperplastic primary vitreous Inferred relationship Existential restriction modifier (core metadata concept)
Persistent hyperplastic primary vitreous of bilateral eyes (disorder) Is a False Persistent hyperplastic primary vitreous Inferred relationship Existential restriction modifier (core metadata concept)
Persistent hyperplastic primary vitreous of left eye (disorder) Is a True Persistent hyperplastic primary vitreous Inferred relationship Existential restriction modifier (core metadata concept)
Persistent hyperplastic primary vitreous of right eye Is a True Persistent hyperplastic primary vitreous Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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