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205675007: Individual with marker heterochromatin (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
315420015 Individual with marker heterochromatin en Synonym Active Entire term case insensitive SNOMED CT core module
591075011 Individual with marker heterochromatin (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 marker heterochromatin Is a Balanced rearrangement and structural marker true Inferred relationship Existential restriction modifier
Individual with marker heterochromatin Occurrence Congenital false Inferred relationship Existential restriction modifier
Individual with marker heterochromatin Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Individual with marker heterochromatin Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Individual with marker heterochromatin Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Individual with marker heterochromatin Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Individual with marker heterochromatin Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Individual with marker heterochromatin 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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