719011002: X-linked intellectual disability Pai type (disorder)

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

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3314661010	X-linked intellectual disability Pai type (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core
3314662015	X-linked intellectual disability Pai type	en	Synonym	Active	Case sensitive	SNOMED CT core
3314663013	This syndrome has characteristics of the association of dysmorphism with intellectual deficit. It has been described in four generations of one family. Premature death was reported in the affected males. Transmission is X-linked recessive and the causative gene has been located to the q28 region of the X chromosome.	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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