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

733473000: 16p13.3 microduplication syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3499509012 Distal trisomy 16p en Synonym Active Only initial character case insensitive SNOMED CT core module
3499510019 Distal duplication 16p en Synonym Active Only initial character case insensitive SNOMED CT core module
3499511015 16p13.3 microduplication syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
3499512010 16p13.3 microduplication syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
16p13.3 microduplication syndrome Is a 16p partial trisomy syndrome false Inferred relationship Existential restriction modifier
16p13.3 microduplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 1
16p13.3 microduplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
16p13.3 microduplication syndrome Finding site Chromosome pair 16 false Inferred relationship Existential restriction modifier 1
16p13.3 microduplication syndrome Is a Duplication of part of short arm of chromosome 16 true Inferred relationship Existential restriction modifier
16p13.3 microduplication syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
16p13.3 microduplication syndrome Finding site Short arm of chromosome true Inferred relationship Existential restriction modifier 1
16p13.3 microduplication syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
16p13.3 microduplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
16p13.3 microduplication syndrome Finding site Chromosome pair 16 true Inferred relationship Existential restriction modifier 2
16p13.3 microduplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 2
16p13.3 microduplication syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start