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205676008: Individual with autosomal fragile site (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
315421016 Individual with autosomal fragile site en Synonym Active Entire term case insensitive SNOMED CT core module
591076012 Individual with autosomal fragile site (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Individual with autosomal fragile site Is a Balanced rearrangement and structural marker true Inferred relationship Existential restriction modifier
Individual with autosomal fragile site Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Individual with autosomal fragile site Occurrence Congenital false Inferred relationship Existential restriction modifier
Individual with autosomal fragile site Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Individual with autosomal fragile site Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Individual with autosomal fragile site Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Individual with autosomal fragile site Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Individual with autosomal fragile site Finding site Chromosome structure 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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