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726106004: X-linked diffuse leiomyomatosis with Alport syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3448200017 X-linked diffuse leiomyomatosis with Alport syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3448201018 X-linked diffuse leiomyomatosis with Alport syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3448202013 X-linked diffuse leiomyomatosis, Alport syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked diffuse leiomyomatosis with Alport syndrome Is a Anomaly of chromosome X true Inferred relationship Existential restriction modifier
X-linked diffuse leiomyomatosis with Alport syndrome Is a Neoplastic disease of uncertain behavior true Inferred relationship Existential restriction modifier
X-linked diffuse leiomyomatosis with Alport syndrome Is a Congenital nephritis true Inferred relationship Existential restriction modifier
X-linked diffuse leiomyomatosis with Alport syndrome Is a Alport syndrome X-linked true Inferred relationship Existential restriction modifier
X-linked diffuse leiomyomatosis with Alport syndrome Associated morphology Chronic inflammation true Inferred relationship Existential restriction modifier 3
X-linked diffuse leiomyomatosis with Alport syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
X-linked diffuse leiomyomatosis with Alport syndrome Finding site Glomerulus structure true Inferred relationship Existential restriction modifier 3
X-linked diffuse leiomyomatosis with Alport syndrome Associated morphology Deletion of long arm true Inferred relationship Existential restriction modifier 4
X-linked diffuse leiomyomatosis with Alport syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 4
X-linked diffuse leiomyomatosis with Alport syndrome Finding site Sex chromosome X true Inferred relationship Existential restriction modifier 4
X-linked diffuse leiomyomatosis with Alport syndrome Associated morphology Leiomyomatosis, no International Classification of Diseases for Oncology subtype false Inferred relationship Existential restriction modifier 5
X-linked diffuse leiomyomatosis with Alport syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 5
X-linked diffuse leiomyomatosis with Alport syndrome Is a Congenital hearing disorder false Inferred relationship Existential restriction modifier
X-linked diffuse leiomyomatosis with Alport syndrome Finding site Structure of auditory system true Inferred relationship Existential restriction modifier 2
X-linked diffuse leiomyomatosis with Alport syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 1
X-linked diffuse leiomyomatosis with Alport syndrome Associated morphology Leiomyomatosis true Inferred relationship Existential restriction modifier 5
X-linked diffuse leiomyomatosis with Alport syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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