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253234004: Congenital heterochromia iridis (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
377139018 Congenital heterochromia iridis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
643968016 Congenital heterochromia iridis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
377139018 Congenital heterochromia iridis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
377139018 Congenital heterochromia iridis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
643968016 Congenital heterochromia iridis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
643968016 Congenital heterochromia iridis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
621311000274111 Kongenitale Heterochromia iridium de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
621321000274116 Kongenitale Irisheterochromie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5070071000241117 hétérochromie congénitale de l'iris fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5070071000241117 hétérochromie congénitale de l'iris fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
621311000274111 Kongenitale Heterochromia iridium de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
621321000274116 Kongenitale Irisheterochromie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital heterochromia iridis (disorder) Is a Congenital anomaly of iris true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital heterochromia iridis (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital heterochromia iridis (disorder) Finding site Iris structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital heterochromia iridis (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital heterochromia iridis (disorder) Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital heterochromia iridis (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital heterochromia iridis (disorder) Finding site Iridial and/or ciliary structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital heterochromia iridis (disorder) Is a Disorder of iris false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital heterochromia iridis (disorder) Finding site Uveal tract structure false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital heterochromia iridis (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital heterochromia iridis (disorder) Finding site Iris structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital heterochromia iridis (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital heterochromia iridis (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital heterochromia iridis (disorder) Finding site Iris structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital heterochromia iridis (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital heterochromia iridis (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital heterochromia iridis (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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