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56332006: Chromosome pair 10 (cell structure)

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
93674011 Chromosome pair 10 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1203735018 Chromosome pair 10 (cell structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
93674011 Chromosome pair 10 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
93674011 Chromosome pair 10 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
794833014 Chromosome pair 10 (body structure) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1203735018 Chromosome pair 10 (cell structure) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1203735018 Chromosome pair 10 (cell structure) en Fully specified name 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 pair 10 Is a Chromosome true Inferred relationship Existential restriction modifier (core metadata concept)
Chromosome pair 10 partie de Nucleus false Additional relationship (core metadata concept) Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
10q partial monosomy (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 2
Anomaly of chromosome pair 10 (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10p partial trisomy syndrome Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10q partial trisomy syndrome Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Complete trisomy 10 syndrome Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Ring chromosome 10 syndrome Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 2
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 3
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 2
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 3
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 2
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 3
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 2
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 3
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 2
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 3
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 3
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 2
10p partial monosomy syndrome (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10q partial monosomy (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Ring chromosome 10 syndrome Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10p partial trisomy syndrome Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10q partial trisomy syndrome Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Complete trisomy 10 syndrome Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 10 (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Ring chromosome 10 syndrome Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Complete trisomy 10 syndrome Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10q partial monosomy (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 10 (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10p partial monosomy syndrome (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10p partial trisomy syndrome Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10q partial trisomy syndrome Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10p partial monosomy syndrome (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 2
10q partial monosomy (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 2
Trisomy 10p (disorder) Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 4
Distal monosomy 10q Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 2
Distal monosomy 10q Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 3
Distal trisomy 10q (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Distal monosomy 10p is a rare chromosomal disorder in which the tip of the short arm (p arm) of chromosome 10 is deleted resulting in a variable phenotype depending on the size of the deletion. The deletion may involve only the terminal 10p15 band, or extend towards the centromere to bands 10p14 or 10p13. Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 2
Distal monosomy 10p is a rare chromosomal disorder in which the tip of the short arm (p arm) of chromosome 10 is deleted resulting in a variable phenotype depending on the size of the deletion. The deletion may involve only the terminal 10p15 band, or extend towards the centromere to bands 10p14 or 10p13. Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 3
Distal limb deficiency with micrognathia syndrome Finding site False Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 5
Hypoparathyroidism, deafness, renal disease syndrome (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 9
Hypoparathyroidism, deafness, renal disease syndrome (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 8
Deletion of part of chromosome 10 (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Partial trisomy of chromosome 10 (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Mosaic trisomy 10 syndrome (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 2
Trisomy 10 (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Mosaic trisomy 10 syndrome (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Non-distal monosomy 10q (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 2
Non-distal monosomy 10q (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Non-distal trisomy 10q (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10q22.3q23.3 microdeletion syndrome Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 2
10q22.3q23.3 microdeletion syndrome Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 10p (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Distal limb deficiency with micrognathia syndrome Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 3
Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
10q22.3q23.3 microduplication syndrome (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 2
Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 3
Proximal duplication of long arm of chromosome 10 (disorder) Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 2
Proximal deletion of long arm of chromosome 10 Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1
Proximal deletion of long arm of chromosome 10 Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 3
Distal monosomy 10q Finding site True Chromosome pair 10 Inferred relationship Existential restriction modifier (core metadata concept) 1

Reference Sets

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