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205675007: Individual with marker heterochromatin (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
315420015 Individual with marker heterochromatin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591075011 Individual with marker heterochromatin (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Individual with marker heterochromatin est un(e) (attribut) Balanced rearrangement and structural marker true Inferred relationship Some
Individual with marker heterochromatin morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Individual with marker heterochromatin localisation d'une constatation (attribut) Chromosome structure (cell structure) false Inferred relationship Some 1
Individual with marker heterochromatin localisation d'une constatation (attribut) Chromosome structure (cell structure) false Inferred relationship Some 1
Individual with marker heterochromatin morphologie associée (attribut) Congenital anomaly false Inferred relationship Some
Individual with marker heterochromatin survenue (attribut) congénital false Inferred relationship Some
Individual with marker heterochromatin morphologie associée (attribut) Alteration of chromosome structure false Inferred relationship Some
Individual with marker heterochromatin localisation d'une constatation (attribut) Chromosome structure (cell structure) true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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