770794008: 11p15.4 microduplication syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Mental state, behaviour and/or psychosocial function finding\Behaviour finding\Intellectual disability\11p15.4 microduplication syndrome
• \Finding of head and neck region\Head finding\...
• \Finding of head region\Finding of face\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\11p15.4 microduplication syndrome
• \Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\11p15.4 microduplication syndrome
• \Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\11p15.4 microduplication syndrome
• \Functional finding\Cognitive function finding\Impaired cognition\Intellectual disability\11p15.4 microduplication syndrome
• \Functional finding\Cognitive function finding\Intellectual ability - finding\Intellectual disability\11p15.4 microduplication syndrome
• \Functional finding\Intelligence finding\Intellectual ability - finding\Intellectual disability\11p15.4 microduplication syndrome
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\11p15.4 microduplication syndrome
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\11p15.4 microduplication syndrome
• \Disease\Chromosomal disorder\Autosomal chromosomal disorder\Autosomal duplication\Trisomy and partial trisomy of autosome\Partial trisomy of chromosome 11\11p15.4 microduplication syndrome
• \Disease\Chromosomal disorder\Duplication of chromosome\Autosomal duplication\Trisomy and partial trisomy of autosome\Partial trisomy of chromosome 11\11p15.4 microduplication syndrome
• \Disease\Chromosomal disorder\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 11\Partial trisomy of chromosome 11\11p15.4 microduplication syndrome
• \Disease\Chromosomal disorder\Congenital chromosomal disease\Trisomy and partial trisomy of autosome\Partial trisomy of chromosome 11\11p15.4 microduplication syndrome
• \Disease\Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\11p15.4 microduplication syndrome
• \Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\11p15.4 microduplication syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\11p15.4 microduplication syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\11p15.4 microduplication syndrome
• \Disease\Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 11\Partial trisomy of chromosome 11\11p15.4 microduplication syndrome
• \Disease\Congenital disease\Congenital chromosomal disease\Trisomy and partial trisomy of autosome\Partial trisomy of chromosome 11\11p15.4 microduplication syndrome
• \Disease\Developmental disorder\Neurodevelopmental disorder\Intellectual disability\11p15.4 microduplication syndrome
• \Disease\Developmental disorder\Developmental hereditary disorder\11p15.4 microduplication syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\11p15.4 microduplication syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\11p15.4 microduplication syndrome

Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3702825016	Trisomy 11p15.4	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3702826015	11p15.4 microduplication syndrome (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3702827012	11p15.4 microduplication syndrome	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3702828019	A rare partial autosomal trisomy characterised by obesity, global developmental delay and intellectual disability, facial dysmorphism (synophrys, high-arched eyebrows, large posteriorly rotated ears, upturned nose, long smooth philtrum, overbite and high palate), large hands and limb hypotonia. Additional features include seizures and behavioural abnormalities.	en	Definition	Active	Case sensitive	SNOMED CT core
3702829010	A rare partial autosomal trisomy characterized by obesity, global developmental delay and intellectual disability, facial dysmorphism (synophrys, high-arched eyebrows, large posteriorly rotated ears, upturned nose, long smooth philtrum, overbite and high palate), large hands and limb hypotonia. Additional features include seizures and behavioral abnormalities.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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