FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

5051002: Anomaly of chromosome pair 9 (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
9456010 Anomaly of chromosome pair 9 en Synonym Active Entire term case insensitive SNOMED CT core module
788307018 Anomaly of chromosome pair 9 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

31 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anomaly of chromosome pair 9 Is a Anomaly of sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 9 Finding site Sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 9 Occurrence Congenital false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 9 Finding site Chromosome pair 9 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 9 Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 9 Is a Anomaly of chromosome pair true Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 9 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 9 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 9 Finding site Chromosome pair 9 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 9 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 9 Finding site Chromosome pair 9 true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 9 Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
9q partial trisomy syndrome Is a False Anomaly of chromosome pair 9 Inferred relationship Existential restriction modifier
9q partial monosomy syndrome Is a False Anomaly of chromosome pair 9 Inferred relationship Existential restriction modifier
Ring chromosome 9 syndrome Is a True Anomaly of chromosome pair 9 Inferred relationship Existential restriction modifier
9p partial monosomy syndrome Is a False Anomaly of chromosome pair 9 Inferred relationship Existential restriction modifier
Partial tetrasomy of chromosome 9 Is a True Anomaly of chromosome pair 9 Inferred relationship Existential restriction modifier
Complete trisomy 9 syndrome Is a False Anomaly of chromosome pair 9 Inferred relationship Existential restriction modifier
9p partial trisomy syndrome Is a False Anomaly of chromosome pair 9 Inferred relationship Existential restriction modifier
Deletion of part of chromosome 9 Is a True Anomaly of chromosome pair 9 Inferred relationship Existential restriction modifier
Partial trisomy of chromosome 9 Is a False Anomaly of chromosome pair 9 Inferred relationship Existential restriction modifier
Trisomy 9 Is a True Anomaly of chromosome pair 9 Inferred relationship Existential restriction modifier
Maternal uniparental disomy of chromosome 9 Is a True Anomaly of chromosome pair 9 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start