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717768004: Alport syndrome X-linked (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3311845012 Alport syndrome X-linked (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3312599010 Alport syndrome X-linked en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3311845012 Alport syndrome X-linked (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3312599010 Alport syndrome X-linked en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3425011001000113 Alport-Syndrom, X-chromosomales de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5996171000241115 syndrome d'Alport lié à l'X fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5996171000241115 syndrome d'Alport lié à l'X fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3425011001000113 Alport-Syndrom, X-chromosomales de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Alport syndrome X-linked (disorder) Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
Alport syndrome X-linked (disorder) Is a Hereditary nephritis false Inferred relationship Existential restriction modifier (core metadata concept)
Alport syndrome X-linked (disorder) Associated morphology inflammation chronique false Inferred relationship Existential restriction modifier (core metadata concept) 1
Alport syndrome X-linked (disorder) Finding site Glomerulus structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Alport syndrome X-linked (disorder) Finding site Structure of auditory system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Alport syndrome X-linked (disorder) Is a Alport syndrome (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Alport syndrome X-linked (disorder) Interprets Hearing true Inferred relationship Existential restriction modifier (core metadata concept) 2
Alport syndrome X-linked (disorder) Is a X-linked dominant hereditary disease (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Alport syndrome X-linked (disorder) Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Alport syndrome X-linked (disorder) Is a X-linked sensorineural hearing loss true Inferred relationship Existential restriction modifier (core metadata concept)
Alport syndrome X-linked (disorder) Associated morphology Chronic inflammatory morphology (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
X-linked diffuse leiomyomatosis with Alport syndrome Is a True Alport syndrome X-linked (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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