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702357000: Chromosome 2q37 deletion syndrome (disorder)

Status: current, Not 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
2995103015 Chromosome 2q37 deletion syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995117012 2q37 deletion syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995538014 Chromosome 2q37 deletion syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995577012 Brachydactyly mental retardation syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995787014 Albright hereditary osteodystrophy-like syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995103015 Chromosome 2q37 deletion syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2995103015 Chromosome 2q37 deletion syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995117012 2q37 deletion syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2995117012 2q37 deletion syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995538014 Chromosome 2q37 deletion syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2995538014 Chromosome 2q37 deletion syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995577012 Brachydactyly mental retardation syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2995577012 Brachydactyly mental retardation syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995787014 Albright hereditary osteodystrophy-like syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2995787014 Albright hereditary osteodystrophy-like syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3413341001000117 Mikrodeletionssyndrom 2q37 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5796011000241116 monosomie 2q37 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5796021000241111 syndrome de délétion du chromosome 2q37 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5796031000241113 syndrome de brachydactylie et déficience intellectuelle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5796011000241116 monosomie 2q37 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5796021000241111 syndrome de délétion du chromosome 2q37 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5796031000241113 syndrome de brachydactylie et déficience intellectuelle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3413341001000117 Mikrodeletionssyndrom 2q37 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chromosome 2q37 deletion syndrome Is a Anomaly of chromosome pair 2 false Inferred relationship Existential restriction modifier (core metadata concept)
Chromosome 2q37 deletion syndrome Is a trouble multisytémique false Inferred relationship Existential restriction modifier (core metadata concept)
Chromosome 2q37 deletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Chromosome 2q37 deletion syndrome Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier (core metadata concept) 1
Chromosome 2q37 deletion syndrome Finding site Chromosome pair 2 (cell structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Chromosome 2q37 deletion syndrome Is a Intelligenzminderung false Inferred relationship Existential restriction modifier (core metadata concept)
Chromosome 2q37 deletion syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Chromosome 2q37 deletion syndrome Is a Deletion of part of long arm of chromosome 2 (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Chromosome 2q37 deletion syndrome Is a Congenital malformation true Inferred relationship Existential restriction modifier (core metadata concept)
Chromosome 2q37 deletion syndrome Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Chromosome 2q37 deletion syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Chromosome 2q37 deletion syndrome Finding site Chromosome pair 2 (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Chromosome 2q37 deletion syndrome Associated morphology Deletion of long arm false Inferred relationship Existential restriction modifier (core metadata concept) 2
Chromosome 2q37 deletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Chromosome 2q37 deletion syndrome Finding site Long arm of chromosome (cell structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Chromosome 2q37 deletion syndrome Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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