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205636003: Whole chromosome monosomy - meiotic nondisjunction (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
315372014 Whole chromosome monosomy - meiotic nondisjunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591032017 Whole chromosome monosomy - meiotic nondisjunction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
315372014 Whole chromosome monosomy - meiotic nondisjunction en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
315372014 Whole chromosome monosomy - meiotic nondisjunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591032017 Whole chromosome monosomy - meiotic nondisjunction (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
591032017 Whole chromosome monosomy - meiotic nondisjunction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4885901000241116 monosomie du chromosome entier-nondisjoction méiotique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4885901000241116 monosomie du chromosome entier-nondisjoction méiotique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Whole chromosome monosomy - meiotic nondisjunction (disorder) Is a Monosomy and deletion from autosome (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Whole chromosome monosomy - meiotic nondisjunction (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Whole chromosome monosomy - meiotic nondisjunction (disorder) Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
Whole chromosome monosomy - meiotic nondisjunction (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Whole chromosome monosomy - meiotic nondisjunction (disorder) Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Whole chromosome monosomy - meiotic nondisjunction (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Whole chromosome monosomy - meiotic nondisjunction (disorder) Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Whole chromosome monosomy - meiotic nondisjunction (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Whole chromosome monosomy - meiotic nondisjunction (disorder) Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier (core metadata concept) 1
Whole chromosome monosomy - meiotic nondisjunction (disorder) Finding site Chromosome true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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