717945001: Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Mental state, behaviour and/or psychosocial function finding\Behaviour finding\Intellectual disability\BRESEK syndrome
• \Functional finding\Cognitive function finding\Impaired cognition\Intellectual disability\BRESEK syndrome
• \Functional finding\Cognitive function finding\Intellectual ability - finding\Intellectual disability\BRESEK syndrome
• \Functional finding\Intelligence finding\Intellectual ability - finding\Intellectual disability\BRESEK syndrome
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\BRESEK syndrome
• \Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked dominant hereditary disease\BRESEK syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\BRESEK syndrome
• \Disease\Developmental disorder\Neurodevelopmental disorder\Intellectual disability\BRESEK syndrome
• \Disease\Developmental disorder\Developmental hereditary disorder\BRESEK syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\BRESEK syndrome

Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3324423016	Brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3324424010	BRESEK syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3324426012	X-linked mental retardation Reish type	en	Synonym	Active	Case sensitive	SNOMED CT core
5155338014	Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
5155339018	Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
5155341017	BRESEK (brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia) syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
5155340016	X-linked syndrome with characteristics of brain anomalies, severe intellectual disability, ectodermal dysplasia, skeletal deformities (vertebral anomalies, scoliosis, polydactyly), ear/eye anomalies (maldevelopment, small optic nerves, low set and large ears with hearing loss) and kidney dysplasia/hypoplasia (giving the acronym BRESEK syndrome). It has been described in two brothers, one of who died shortly after birth. One of the brothers also had Hirschsprung disease and Cleft palate/cryptorchidism (giving the acronym: BRESHECK syndrome). Transmission is X-linked dominant.	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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