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205636003: Whole chromosome monosomy - meiotic nondisjunction (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
315372014 Whole chromosome monosomy - meiotic nondisjunction en Synonym Active Entire term case insensitive SNOMED CT core module
591032017 Whole chromosome monosomy - meiotic nondisjunction (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
Whole chromosome monosomy - meiotic nondisjunction Is a Monosomy and deletion from autosome true Inferred relationship Existential restriction modifier
Whole chromosome monosomy - meiotic nondisjunction Occurrence Congenital false Inferred relationship Existential restriction modifier
Whole chromosome monosomy - meiotic nondisjunction Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Whole chromosome monosomy - meiotic nondisjunction Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Whole chromosome monosomy - meiotic nondisjunction Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Whole chromosome monosomy - meiotic nondisjunction Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Whole chromosome monosomy - meiotic nondisjunction Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Whole chromosome monosomy - meiotic nondisjunction Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Whole chromosome monosomy - meiotic nondisjunction Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier 1
Whole chromosome monosomy - meiotic nondisjunction 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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