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205638002: Monosomy 21, mosaicism (disorder)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
315377015 Monosomy 21, mosaicism en Synonym Active Case insensitive SNOMED CT core
591035015 Monosomy 21, mosaicism (disorder) en Fully specified name Active Case insensitive SNOMED CT core

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 Some
Monosomy 21, mosaicism Finding site Chromosome structure false Inferred relationship Some 1
Monosomy 21, mosaicism Associated morphology Congenital anomaly false Inferred relationship Some 1
Monosomy 21, mosaicism Associated morphology Congenital anomaly false Inferred relationship Some
Monosomy 21, mosaicism Finding site Chromosome structure false Inferred relationship Some 1
Monosomy 21, mosaicism Associated morphology Alteration of chromosome structure false Inferred relationship Some
Monosomy 21, mosaicism Occurrence Congenital false Inferred relationship Some
Monosomy 21, mosaicism Occurrence Congenital true Inferred relationship Some 1
Monosomy 21, mosaicism Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Some 1
Monosomy 21, mosaicism Finding site Chromosome true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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