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

768713003: 15q13.3 microduplication syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3686603014 15q13.3 microduplication syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3686604015 15q13.3 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
15q13.3 microduplication syndrome Finding site Chromosome pair 15 false Inferred relationship Existential restriction modifier 1
15q13.3 microduplication syndrome Is a 15q partial trisomy syndrome false Inferred relationship Existential restriction modifier
15q13.3 microduplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 1
15q13.3 microduplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
15q13.3 microduplication syndrome Is a Partial duplication of long arm of chromosome 15 true Inferred relationship Existential restriction modifier
15q13.3 microduplication syndrome Is a Congenital malformation true Inferred relationship Existential restriction modifier
15q13.3 microduplication syndrome Finding site Long arm of chromosome true Inferred relationship Existential restriction modifier 1
15q13.3 microduplication syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
15q13.3 microduplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
15q13.3 microduplication syndrome Finding site Chromosome pair 15 true Inferred relationship Existential restriction modifier 2
15q13.3 microduplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 2
15q13.3 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