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

771337007: 1q21.1 microduplication syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3705811011 1q21.1 microduplication syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3705812016 Trisomy 1q21.1 en Synonym Active Entire term case insensitive SNOMED CT core module
3705813014 1q21.1 microduplication syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
1q21.1 microduplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
1q21.1 microduplication syndrome Finding site Chromosome pair 1 true Inferred relationship Existential restriction modifier 2
1q21.1 microduplication syndrome Finding site Long arm of chromosome true Inferred relationship Existential restriction modifier 1
1q21.1 microduplication syndrome Is a Partial trisomy of long arm of chromosome 1 true Inferred relationship Existential restriction modifier
1q21.1 microduplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 2
1q21.1 microduplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
1q21.1 microduplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 1
1q21.1 microduplication syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
1q21.1 microduplication syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
1q21.1 microduplication syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start