719808002: Chromosome Xp11.3 microdeletion syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Mental state, behaviour and/or psychosocial function finding\Behaviour finding\Intellectual disability\Chromosome Xp11.3 microdeletion syndrome

\Finding of head and neck region\Head finding\...

\Finding of head region\Disorder of eye region\Disorder of eye\Anomaly of eye\Degenerative disorder of eye\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Finding of head region\Disorder of eye region\Disorder of eye\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina\Retinal disorder\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Finding of head region\Globe finding\Retina finding\Retinal disorder\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Finding of head region\Globe finding\Disorder of eye\Anomaly of eye\Degenerative disorder of eye\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Finding of head region\Globe finding\Disorder of eye\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina\Retinal disorder\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome

\Disorder of head\Disorder of eye region\Disorder of eye\...

\Anomaly of eye\Degenerative disorder of eye\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome

\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina\Retinal disorder\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome

\Eye / vision finding\Globe finding\Retina finding\Retinal disorder\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Eye / vision finding\Globe finding\Disorder of eye\Anomaly of eye\Degenerative disorder of eye\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Eye / vision finding\Globe finding\Disorder of eye\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina\Retinal disorder\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Eye / vision finding\Visual system disorder\Disorder of eye region\Disorder of eye\Anomaly of eye\Degenerative disorder of eye\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Eye / vision finding\Visual system disorder\Disorder of eye region\Disorder of eye\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina\Retinal disorder\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Eye / vision finding\Visual system disorder\Hereditary disorder of the visual system\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome

\Functional finding\Cognitive function finding\Impaired cognition\Intellectual disability\Chromosome Xp11.3 microdeletion syndrome
\Functional finding\Cognitive function finding\Intellectual ability - finding\Intellectual disability\Chromosome Xp11.3 microdeletion syndrome
\Functional finding\Intelligence finding\Intellectual ability - finding\Intellectual disability\Chromosome Xp11.3 microdeletion syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the visual system\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Chromosome Xp11.3 microdeletion syndrome
\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked recessive hereditary disease\Chromosome Xp11.3 microdeletion syndrome
\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Disease\Chromosomal disorder\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\Anomaly of chromosome X\Chromosome Xp11.3 microdeletion syndrome
\Disease\Degenerative disorder\Degenerative disorder of eye\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the visual system\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of eye\Anomaly of eye\Degenerative disorder of eye\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of eye\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina\Retinal disorder\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Disease\Disorder of body system\Visual system disorder\Hereditary disorder of the visual system\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Disease\Disorder of head\Disorder of eye region\Disorder of eye\Anomaly of eye\Degenerative disorder of eye\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Disease\Disorder of head\Disorder of eye region\Disorder of eye\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina\Retinal disorder\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Retinitis pigmentosa\X-linked retinitis pigmentosa\Chromosome Xp11.3 microdeletion syndrome
\Disease\Congenital disease\Congenital anomaly\Chromosome Xp11.3 microdeletion syndrome
\Disease\Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\Anomaly of chromosome X\Chromosome Xp11.3 microdeletion syndrome
\Disease\Developmental disorder\Neurodevelopmental disorder\Intellectual disability\Chromosome Xp11.3 microdeletion syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Chromosome Xp11.3 microdeletion syndrome
\Disease\Developmental disorder\Congenital anomaly\Chromosome Xp11.3 microdeletion syndrome

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

Descriptions:

Id Description Lang Type Status Case? Module

3317982011 Chromosome Xp11.3 microdeletion syndrome (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

3317983018 Chromosome Xp11.3 microdeletion syndrome en Synonym Active Initial character case insensitive SNOMED CT core

3317984012 Aldred syndrome en Synonym Active Case sensitive SNOMED CT core

3317985013 This syndrome has characteristics of moderate intellectual deficit and severe, early-onset retinitis pigmentosa. It has been described in five males spanning three generations of one family. Some patients also had microcephaly. It is transmitted as an X-linked recessive trait. en Definition Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Chromosome Xp11.3 microdeletion syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1
Chromosome Xp11.3 microdeletion syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Some
Chromosome Xp11.3 microdeletion syndrome	Occurrence	Congenital	true	Inferred relationship	Some	1
Chromosome Xp11.3 microdeletion syndrome	Is a	X-linked retinitis pigmentosa	true	Inferred relationship	Some
Chromosome Xp11.3 microdeletion syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Some	2
Chromosome Xp11.3 microdeletion syndrome	Is a	Congenital anomaly	true	Inferred relationship	Some
Chromosome Xp11.3 microdeletion syndrome	Finding site	Retinal structure	true	Inferred relationship	Some	3
Chromosome Xp11.3 microdeletion syndrome	Finding site	Short arm of chromosome	true	Inferred relationship	Some	1
Chromosome Xp11.3 microdeletion syndrome	Associated morphology	Partial monosomy	true	Inferred relationship	Some	2
Chromosome Xp11.3 microdeletion syndrome	Associated morphology	Dystrophy	true	Inferred relationship	Some	3
Chromosome Xp11.3 microdeletion syndrome	Associated morphology	Partial monosomy	true	Inferred relationship	Some	1
Chromosome Xp11.3 microdeletion syndrome	Is a	X-linked recessive hereditary disease	true	Inferred relationship	Some
Chromosome Xp11.3 microdeletion syndrome	Interprets	Intellectual ability	true	Inferred relationship	Some	4
Chromosome Xp11.3 microdeletion syndrome	Has interpretation	Impaired	true	Inferred relationship	Some	4
Chromosome Xp11.3 microdeletion syndrome	Interprets	Adaptation behaviour	true	Inferred relationship	Some	5
Chromosome Xp11.3 microdeletion syndrome	Has interpretation	Impaired	true	Inferred relationship	Some	5
Chromosome Xp11.3 microdeletion syndrome	Is a	Intellectual disability	false	Inferred relationship	Some
Chromosome Xp11.3 microdeletion syndrome	Is a	Anomaly of chromosome X	true	Inferred relationship	Some
Chromosome Xp11.3 microdeletion syndrome	Is a	X-linked hereditary disease	false	Inferred relationship	Some
Chromosome Xp11.3 microdeletion syndrome	Is a	Deletion of part of autosome	false	Inferred relationship	Some
Chromosome Xp11.3 microdeletion syndrome	Associated morphology	Deletion of short arm	false	Inferred relationship	Some	2
Chromosome Xp11.3 microdeletion syndrome	Occurrence	Congenital	true	Inferred relationship	Some	2
Chromosome Xp11.3 microdeletion syndrome	Finding site	Sex chromosome X	true	Inferred relationship	Some	2
Chromosome Xp11.3 microdeletion syndrome	Associated morphology	Partial monosomy	false	Inferred relationship	Some	3
Chromosome Xp11.3 microdeletion syndrome	Occurrence	Congenital	false	Inferred relationship	Some	3
Chromosome Xp11.3 microdeletion syndrome	Finding site	Sex chromosome X	false	Inferred relationship	Some	3
Chromosome Xp11.3 microdeletion syndrome	Is a	Intellectual disability	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3317982011	Chromosome Xp11.3 microdeletion syndrome (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3317983018	Chromosome Xp11.3 microdeletion syndrome	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3317984012	Aldred syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3317985013	This syndrome has characteristics of moderate intellectual deficit and severe, early-onset retinitis pigmentosa. It has been described in five males spanning three generations of one family. Some patients also had microcephaly. It is transmitted as an X-linked recessive trait.	en	Definition	Active	Case sensitive	SNOMED CT core