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205676008: Individual with autosomal fragile site (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
315421016 Individual with autosomal fragile site en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591076012 Individual with autosomal fragile site (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
315421016 Individual with autosomal fragile site en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
315421016 Individual with autosomal fragile site en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591076012 Individual with autosomal fragile site (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
591076012 Individual with autosomal fragile site (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4886341000241112 sujet avec site autosomique fragile fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4886341000241112 sujet avec site autosomique fragile fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Individual with autosomal fragile site (disorder) Is a Balanced rearrangement and structural marker (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Individual with autosomal fragile site (disorder) Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
Individual with autosomal fragile site (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Individual with autosomal fragile site (disorder) Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Individual with autosomal fragile site (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Individual with autosomal fragile site (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Individual with autosomal fragile site (disorder) Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Individual with autosomal fragile site (disorder) Finding site Chromosome structure (cell structure) 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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