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254269007: Whole chromosome trisomy 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
378502011 Whole chromosome trisomy - meiotic nondisjunction en Synonym Inactive Entire term case insensitive SNOMED CT core module
645137017 Whole chromosome trisomy - meiotic nondisjunction (disorder) en Fully specified name Inactive Entire term case insensitive SNOMED CT core module
3661467010 Whole chromosome trisomy meiotic nondisjunction (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3661470014 Whole chromosome trisomy meiotic nondisjunction en Synonym Active Entire term case insensitive SNOMED CT core module

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Whole chromosome trisomy meiotic nondisjunction Is a Trisomy and partial trisomy of autosome true Inferred relationship Existential restriction modifier
Whole chromosome trisomy meiotic nondisjunction Occurrence Congenital false Inferred relationship Existential restriction modifier
Whole chromosome trisomy meiotic nondisjunction Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Whole chromosome trisomy meiotic nondisjunction Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Whole chromosome trisomy meiotic nondisjunction Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Whole chromosome trisomy meiotic nondisjunction Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Whole chromosome trisomy meiotic nondisjunction Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Whole chromosome trisomy meiotic nondisjunction Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Whole chromosome trisomy meiotic nondisjunction Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Whole chromosome trisomy meiotic nondisjunction Finding site Chromosome structure true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Trisomy 21- meiotic nondisjunction Is a True Whole chromosome trisomy meiotic nondisjunction Inferred relationship Existential restriction modifier
Trisomy 18 - meiotic nondisjunction Is a True Whole chromosome trisomy meiotic nondisjunction Inferred relationship Existential restriction modifier
Trisomy 13, meiotic nondisjunction Is a True Whole chromosome trisomy meiotic nondisjunction Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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