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768713003: 15q13.3 microduplication syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3686603014 15q13.3 microduplication syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3686604015 15q13.3 microduplication syndrome en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
15q13.3 microduplication syndrome Is a Partial duplication of long arm of chromosome 15 true Inferred relationship Some
15q13.3 microduplication syndrome Is a Congenital anomaly true Inferred relationship Some
15q13.3 microduplication syndrome Finding site Long arm of chromosome true Inferred relationship Some 1
15q13.3 microduplication syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
15q13.3 microduplication syndrome Occurrence Congenital true Inferred relationship Some 2
15q13.3 microduplication syndrome Finding site Chromosome pair 15 true Inferred relationship Some 2
15q13.3 microduplication syndrome Associated morphology Partial trisomy true Inferred relationship Some 2
15q13.3 microduplication syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
15q13.3 microduplication syndrome Finding site Chromosome pair 15 false Inferred relationship Some 1
15q13.3 microduplication syndrome Is a 15q partial trisomy syndrome false Inferred relationship Some
15q13.3 microduplication syndrome Associated morphology Partial trisomy true Inferred relationship Some 1
15q13.3 microduplication syndrome Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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