783061008: Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Mental state, behaviour and/or psychosocial function finding\Behaviour finding\Intellectual disability\WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \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\WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Functional finding\Cognitive function finding\Impaired cognition\Intellectual disability\WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Functional finding\Cognitive function finding\Intellectual ability - finding\Intellectual disability\WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Functional finding\Intelligence finding\Intellectual ability - finding\Intellectual disability\WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Disease\Genetic disease\WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Disease\Chromosomal disorder\Congenital chromosomal disease\Anomaly of chromosome pair\Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 10\10p partial monosomy syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Disease\Chromosomal disorder\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 10\Deletion of part of chromosome 10\10p partial monosomy syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Disease\Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Disease\Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 10\10p partial monosomy syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Disease\Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 10\Deletion of part of chromosome 10\10p partial monosomy syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Disease\Developmental disorder\Neurodevelopmental disorder\Intellectual disability\WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
• \Disease\Developmental disorder\Developmental delay\WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome\Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3757287015	Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3757288013	Monosomy 10p11.21p12.31	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3757289017	Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3757290014	10p12p11 microdeletion syndrome	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3757291013	Deletion 10p11.21p12.31	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3757292018	Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3757293011	A rare genetic syndromic intellectual disability characterised by developmental delay, hypotonia, speech delay, mild to moderate intellectual disability, abnormal behaviour (autistic, aggressive, hyperactive) and dysmorphic facial features, including synophrys or thick eyebrows, deep set eyes, bulbous nasal tip and full cheeks. Congenital heart and brain anomalies, visual and hearing impairment are also common.	en	Definition	Active	Case sensitive	SNOMED CT core
3757294017	A rare genetic syndromic intellectual disability characterized by developmental delay, hypotonia, speech delay, mild to moderate intellectual disability, abnormal behavior (autistic, aggressive, hyperactive) and dysmorphic facial features, including synophrys or thick eyebrows, deep set eyes, bulbous nasal tip and full cheeks. Congenital heart and brain anomalies, visual and hearing impairment are also common.	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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