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205638002: Monosomy 21, mosaicism (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
315377015 Monosomy 21, mosaicism en Synonym Active Entire term case insensitive SNOMED CT core module
591035015 Monosomy 21, mosaicism (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
Monosomy 21, mosaicism Is a Monosomy and deletion from autosome true Inferred relationship Existential restriction modifier
Monosomy 21, mosaicism Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Monosomy 21, mosaicism Occurrence Congenital false Inferred relationship Existential restriction modifier
Monosomy 21, mosaicism Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Monosomy 21, mosaicism Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Monosomy 21, mosaicism Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Monosomy 21, mosaicism Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Monosomy 21, mosaicism Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Monosomy 21, mosaicism Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier 1
Monosomy 21, mosaicism Finding site Chromosome 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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