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32299009: Anomaly of chromosome pair 2 (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
53956010 Anomaly of chromosome pair 2 en Synonym Active Entire term case insensitive SNOMED CT core module
53957018 Anomaly of chromosome pair 2, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
763565016 Anomaly of chromosome pair 2 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

30 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anomaly of chromosome pair 2 Is a Anomaly of sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 2 Finding site Sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 2 Occurrence Congenital false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 2 Finding site Chromosome pair 2 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 2 Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 2 Is a Anomaly of chromosome pair true Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 2 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 2 Finding site Chromosome pair 2 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 2 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 2 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 2 Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 2 Finding site Chromosome pair 2 true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
2p partial trisomy syndrome Is a False Anomaly of chromosome pair 2 Inferred relationship Existential restriction modifier
2q partial trisomy syndrome Is a False Anomaly of chromosome pair 2 Inferred relationship Existential restriction modifier
Chromosome 2q37 deletion syndrome Is a False Anomaly of chromosome pair 2 Inferred relationship Existential restriction modifier
2q31.1 microdeletion syndrome Is a False Anomaly of chromosome pair 2 Inferred relationship Existential restriction modifier
2p15p16.1 microdeletion syndrome Is a False Anomaly of chromosome pair 2 Inferred relationship Existential restriction modifier
2p21 microdeletion syndrome Is a False Anomaly of chromosome pair 2 Inferred relationship Existential restriction modifier
2q23.1 microdeletion syndrome Is a False Anomaly of chromosome pair 2 Inferred relationship Existential restriction modifier
2q24 microdeletion syndrome Is a False Anomaly of chromosome pair 2 Inferred relationship Existential restriction modifier
2q32q33 microdeletion syndrome Is a False Anomaly of chromosome pair 2 Inferred relationship Existential restriction modifier
Deletion of part of chromosome 2 Is a True Anomaly of chromosome pair 2 Inferred relationship Existential restriction modifier
Partial trisomy of chromosome 2 Is a True Anomaly of chromosome pair 2 Inferred relationship Existential restriction modifier
Mosaic trisomy 2 syndrome Is a True Anomaly of chromosome pair 2 Inferred relationship Existential restriction modifier
Ring chromosome 2 syndrome Is a True Anomaly of chromosome pair 2 Inferred relationship Existential restriction modifier
Maternal uniparental disomy of chromosome 2 Is a True Anomaly of chromosome pair 2 Inferred relationship Existential restriction modifier
Overgrowth syndrome with 2q37 translocation Is a True Anomaly of chromosome pair 2 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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