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699306003: Chromosome 1p36 deletion syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2983611014 Distal monosomy 1p36 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983665014 Monosomy 1p36 syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983669015 Chromosome 1p36 deletion syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983672010 Chromosome 1p36 deletion syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983739016 1p36 deletion syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chromosome 1p36 deletion syndrome (disorder) localisation d'une constatation (attribut) Short arm of chromosome (cell structure) true Inferred relationship Some 1
Chromosome 1p36 deletion syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Chromosome 1p36 deletion syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Chromosome 1p36 deletion syndrome (disorder) morphologie associée (attribut) Partial monosomy (morphologic abnormality) true Inferred relationship Some 2
Chromosome 1p36 deletion syndrome (disorder) est un(e) (attribut) Congenital malformation true Inferred relationship Some
Chromosome 1p36 deletion syndrome (disorder) est un(e) (attribut) Anomaly of chromosome pair 1 false Inferred relationship Some
Chromosome 1p36 deletion syndrome (disorder) survenue (attribut) congénital false Inferred relationship Some
Chromosome 1p36 deletion syndrome (disorder) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some
Chromosome 1p36 deletion syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Chromosome 1p36 deletion syndrome (disorder) localisation d'une constatation (attribut) Chromosome pair 1 (cell structure) false Inferred relationship Some 1
Chromosome 1p36 deletion syndrome (disorder) est un(e) (attribut) Deletion of part of autosome false Inferred relationship Some
Chromosome 1p36 deletion syndrome (disorder) morphologie associée (attribut) Partial monosomy (morphologic abnormality) true Inferred relationship Some 1
Chromosome 1p36 deletion syndrome (disorder) est un(e) (attribut) Deletion of part of chromosome 1 (disorder) false Inferred relationship Some
Chromosome 1p36 deletion syndrome (disorder) est un(e) (attribut) 1p partial monosomy true Inferred relationship Some
Chromosome 1p36 deletion syndrome (disorder) morphologie associée (attribut) Deletion of short arm false Inferred relationship Some 2
Chromosome 1p36 deletion syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Chromosome 1p36 deletion syndrome (disorder) localisation d'une constatation (attribut) Chromosome pair 1 (cell structure) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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