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95484004: Congenital pigmentation of lens (disorder)


Status: current, 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
158163010 Congenital pigmentation of lens en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
839647011 Congenital pigmentation of lens (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
158163010 Congenital pigmentation of lens en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
158163010 Congenital pigmentation of lens en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
839647011 Congenital pigmentation of lens (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
839647011 Congenital pigmentation of lens (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
513031000274117 Kongenitale Pigmentierung der Augenlinse de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
626991000274114 Kongenitale Pigmentierung der Linse de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4730711000241115 pigmentation congénitale du cristallin fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4730711000241115 pigmentation congénitale du cristallin fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
513031000274117 Kongenitale Pigmentierung der Augenlinse de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
626991000274114 Kongenitale Pigmentierung der Linse de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital pigmentation of lens (disorder) Is a Congenital anomaly of lens shape false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pigmentation of lens (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pigmentation of lens (disorder) Associated morphology Congenital pigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pigmentation of lens (disorder) Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pigmentation of lens (disorder) Finding site Structure of lens of eye (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pigmentation of lens (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pigmentation of lens (disorder) Finding site Structure of lens of eye (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pigmentation of lens (disorder) Finding site Structure of lens of eye (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital pigmentation of lens (disorder) Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital pigmentation of lens (disorder) Finding site Structure of lens of eye (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital pigmentation of lens (disorder) Finding site Structure of lens of eye (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pigmentation of lens (disorder) Finding site Structure of lens of eye (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital pigmentation of lens (disorder) Finding site Structure of lens of eye (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pigmentation of lens (disorder) Finding site Structure of lens of eye (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pigmentation of lens (disorder) Finding site Structure of lens of eye (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital pigmentation of lens (disorder) Finding site Structure of lens of eye (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital pigmentation of lens (disorder) Finding site Structure of lens of eye (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pigmentation of lens (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital pigmentation of lens (disorder) Finding site Structure of lens of eye (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital pigmentation of lens (disorder) Associated morphology Congenital abnormal shape false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital pigmentation of lens (disorder) Is a Kongenitale Anomalie der Linse true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pigmentation of lens (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital pigmentation of lens (disorder) Associated morphology Congenital pigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital pigmentation of lens (disorder) Finding site Structure of lens of eye (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital pigmentation of lens (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pigmentation of lens (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pigmentation of lens (disorder) Associated morphology Structure showing abnormal deposition of pigment (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pigmentation of lens (disorder) Is a Disorder of pigmentation (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pigmentation of lens (disorder) Is a Lesion of eye (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pigmentation of lens (disorder) Is a Degenerative disorder of eye (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital anterior capsular pigmentation Is a True Congenital pigmentation of lens (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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