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2893009: Anomaly of chromosome pair 10 (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
5897015 Anomaly of chromosome pair 10 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
759666019 Anomaly of chromosome pair 10 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
965891000172114 anomalie du chromosome 10 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

22 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anomaly of chromosome pair 10 Is a Anomaly of sex chromosome false Inferred relationship Some
Anomaly of chromosome pair 10 Occurrence Congenital false Inferred relationship Some
Anomaly of chromosome pair 10 Finding site Sex chromosome false Inferred relationship Some
Anomaly of chromosome pair 10 Finding site Chromosome pair 10 false Inferred relationship Some 1
Anomaly of chromosome pair 10 Associated morphology Alteration of chromosome structure false Inferred relationship Some
Anomaly of chromosome pair 10 Is a Anomaly of chromosome pair true Inferred relationship Some
Anomaly of chromosome pair 10 Associated morphology anomalie congénitale false Inferred relationship Some 1
Anomaly of chromosome pair 10 Associated morphology anomalie congénitale false Inferred relationship Some
Anomaly of chromosome pair 10 Finding site Chromosome pair 10 false Inferred relationship Some 1
Anomaly of chromosome pair 10 Occurrence Congenital true Inferred relationship Some 1
Anomaly of chromosome pair 10 Finding site Chromosome pair 10 true Inferred relationship Some 1
Anomaly of chromosome pair 10 Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
10q partial monosomy (disorder) Is a False Anomaly of chromosome pair 10 Inferred relationship Some
10p partial trisomy syndrome Is a False Anomaly of chromosome pair 10 Inferred relationship Some
10p partial monosomy syndrome (disorder) Is a False Anomaly of chromosome pair 10 Inferred relationship Some
10q partial trisomy syndrome Is a False Anomaly of chromosome pair 10 Inferred relationship Some
Complete trisomy 10 syndrome Is a False Anomaly of chromosome pair 10 Inferred relationship Some
An autosomal anomaly characterised by variable clinical features, depending on the size and precise location of deleted chromosome segments. Most patients present with developmental delay, intellectual disability, growth retardation, microcephaly, clinodactyly, and dysmorphic features. Congenital heart disease and genitourinary anomalies were reported in some cases. Is a True Anomaly of chromosome pair 10 Inferred relationship Some
Trisomy 10p is a syndrome of mental retardation/multiple congenital malformations (MR-MCA) that is caused by the total or partial duplication of the short arm of chromosome 10. Is a False Anomaly of chromosome pair 10 Inferred relationship Some
Deletion of part of chromosome 10 (disorder) Is a True Anomaly of chromosome pair 10 Inferred relationship Some
Partial trisomy of chromosome 10 (disorder) Is a False Anomaly of chromosome pair 10 Inferred relationship Some
Trisomy 10 Is a True Anomaly of chromosome pair 10 Inferred relationship Some

This concept is not in any reference sets

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