FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

37535007: Anomaly of chromosome pair 12 (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
62616016 Anomaly of chromosome pair 12 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
769413013 Anomaly of chromosome pair 12 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
62616016 Anomaly of chromosome pair 12 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
62616016 Anomaly of chromosome pair 12 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
769413013 Anomaly of chromosome pair 12 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
769413013 Anomaly of chromosome pair 12 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
871971000172119 anomalie du chromosome 12 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
871971000172119 anomalie du chromosome 12 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 12 Is a Anomaly of sex chromosome false Inferred relationship Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 12 Finding site Sex chromosome false Inferred relationship Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 12 Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 12 Finding site Chromosome pair 12 false Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 12 Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 12 Is a Anomaly of chromosome pair true Inferred relationship Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 12 Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 12 Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 12 Finding site Chromosome pair 12 false Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 12 Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 12 Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 12 Finding site Chromosome pair 12 true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
12p partial trisomy syndrome Is a False Anomaly of chromosome pair 12 Inferred relationship Existential restriction modifier (core metadata concept)
12p partial monosomy syndrome Is a False Anomaly of chromosome pair 12 Inferred relationship Existential restriction modifier (core metadata concept)
12q partial trisomy syndrome Is a False Anomaly of chromosome pair 12 Inferred relationship Existential restriction modifier (core metadata concept)
Tetrasomy 12p syndrome (disorder) Is a True Anomaly of chromosome pair 12 Inferred relationship Existential restriction modifier (core metadata concept)
Ulnar mammary syndrome Is a True Anomaly of chromosome pair 12 Inferred relationship Existential restriction modifier (core metadata concept)
12q14 microdeletion syndrome (disorder) Is a False Anomaly of chromosome pair 12 Inferred relationship Existential restriction modifier (core metadata concept)
Deletion of part of chromosome 12 (disorder) Is a True Anomaly of chromosome pair 12 Inferred relationship Existential restriction modifier (core metadata concept)
Partial trisomy of chromosome 12 (disorder) Is a False Anomaly of chromosome pair 12 Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 12 (disorder) Is a True Anomaly of chromosome pair 12 Inferred relationship Existential restriction modifier (core metadata concept)
Ring chromosome 12 syndrome Is a True Anomaly of chromosome pair 12 Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start