718914002: X-linked intellectual disability Van Esch type (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Mental state, behavior and/or psychosocial function finding (finding)\Behavior finding\Intellectual disability\X-linked intellectual disability Van Esch type (disorder)

\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of reproductive system\Reproductive system hereditary disorder\X-linked intellectual disability Van Esch type (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of endocrine gonad\Hypogonadism\Primary hypogonadism (disorder)\X-linked intellectual disability Van Esch type (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding (finding)\Genital finding\Disorder of endocrine gonad\Hypogonadism\Primary hypogonadism (disorder)\X-linked intellectual disability Van Esch type (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding (finding)\Disorder of the genitourinary system (disorder)\Disorder of reproductive system\Reproductive system hereditary disorder\X-linked intellectual disability Van Esch type (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding (finding)\Disorder of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of endocrine gonad\Hypogonadism\Primary hypogonadism (disorder)\X-linked intellectual disability Van Esch type (disorder)
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of reproductive system\Reproductive system hereditary disorder\X-linked intellectual disability Van Esch type (disorder)
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of endocrine gonad\Hypogonadism\Primary hypogonadism (disorder)\X-linked intellectual disability Van Esch type (disorder)

\Functional finding\Cognitive function finding (finding)\Impaired cognition (finding)\Intellectual disability\X-linked intellectual disability Van Esch type (disorder)
\Functional finding\Cognitive function finding (finding)\Intellectual ability - finding\Intellectual disability\X-linked intellectual disability Van Esch type (disorder)
\Functional finding\Intelligence finding\Intellectual ability - finding\Intellectual disability\X-linked intellectual disability Van Esch type (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Reproductive system hereditary disorder\X-linked intellectual disability Van Esch type (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\X-linked intellectual disability Van Esch type (disorder)
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\X-linked intellectual disability Van Esch type (disorder)
\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked recessive hereditary disease\X-linked intellectual disability Van Esch type (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\X-linked intellectual disability Van Esch type (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Reproductive system hereditary disorder\X-linked intellectual disability Van Esch type (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\X-linked intellectual disability Van Esch type (disorder)
\Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system (disorder)\X-linked intellectual disability Van Esch type (disorder)
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of endocrine gonad\Hypogonadism\Primary hypogonadism (disorder)\X-linked intellectual disability Van Esch type (disorder)
\Disease\Disorder of body system\Disorder of the genitourinary system (disorder)\Disorder of reproductive system\Reproductive system hereditary disorder\X-linked intellectual disability Van Esch type (disorder)
\Disease\Disorder of body system\Disorder of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of endocrine gonad\Hypogonadism\Primary hypogonadism (disorder)\X-linked intellectual disability Van Esch type (disorder)
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of reproductive system\Reproductive system hereditary disorder\X-linked intellectual disability Van Esch type (disorder)
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of reproductive system\Disorder of endocrine gonad\Hypogonadism\Primary hypogonadism (disorder)\X-linked intellectual disability Van Esch type (disorder)
\Disease\Developmental disorder\Neurodevelopmental disorder\Intellectual disability\X-linked intellectual disability Van Esch type (disorder)
\Disease\Developmental disorder\Developmental hereditary disorder\X-linked intellectual disability Van Esch type (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3314402011 X-linked intellectual disability Van Esch type (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

3314403018 X-linked intellectual disability Van Esch type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

5401909016 A rare, genetic, syndromic intellectual disability characterized by developmental delay, mild to moderate intellectual disability, low birth weight, moderate to severe short stature, microcephaly and variable hypergonadotropic hypogonadism. Mild facial dysmorphism include upslanted palpebral fissures and prominent nasal bridge. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5401910014 A rare, genetic, syndromic intellectual disability characterised by developmental delay, mild to moderate intellectual disability, low birth weight, moderate to severe short stature, microcephaly and variable hypergonadotropic hypogonadism. Mild facial dysmorphism include upslanted palpebral fissures and prominent nasal bridge. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
X-linked intellectual disability Van Esch type (disorder)	Is a	Mental retardation	false	Inferred relationship	Some
X-linked intellectual disability Van Esch type (disorder)	Is a	X-linked hereditary disease	false	Inferred relationship	Some
X-linked intellectual disability Van Esch type (disorder)	Is a	Hereditary disorder of endocrine system (disorder)	true	Inferred relationship	Some
X-linked intellectual disability Van Esch type (disorder)	Is a	Reproductive system hereditary disorder	true	Inferred relationship	Some
X-linked intellectual disability Van Esch type (disorder)	Is a	Primary hypogonadism (disorder)	true	Inferred relationship	Some
X-linked intellectual disability Van Esch type (disorder)	Finding site	Gonadal endocrine structure	false	Inferred relationship	Some
X-linked intellectual disability Van Esch type (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
X-linked intellectual disability Van Esch type (disorder)	Finding site	Gonadal endocrine structure	true	Inferred relationship	Some	1
X-linked intellectual disability Van Esch type (disorder)	Is a	Intellectual disability	true	Inferred relationship	Some
X-linked intellectual disability Van Esch type (disorder)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	2
X-linked intellectual disability Van Esch type (disorder)	Is a	Congenital disease (disorder)	true	Inferred relationship	Some
X-linked intellectual disability Van Esch type (disorder)	Is a	Developmental hereditary disorder	true	Inferred relationship	Some
X-linked intellectual disability Van Esch type (disorder)	Is a	X-linked recessive hereditary disease	true	Inferred relationship	Some
X-linked intellectual disability Van Esch type (disorder)	Interprets	Intellectual ability (observable entity)	true	Inferred relationship	Some	3
X-linked intellectual disability Van Esch type (disorder)	Has interpretation	Impaired	true	Inferred relationship	Some	3
X-linked intellectual disability Van Esch type (disorder)	Interprets	Adaptation behavior (observable entity)	true	Inferred relationship	Some	4
X-linked intellectual disability Van Esch type (disorder)	Has interpretation	Impaired	true	Inferred relationship	Some	4

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3314402011	X-linked intellectual disability Van Esch type (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3314403018	X-linked intellectual disability Van Esch type	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401909016	A rare, genetic, syndromic intellectual disability characterized by developmental delay, mild to moderate intellectual disability, low birth weight, moderate to severe short stature, microcephaly and variable hypergonadotropic hypogonadism. Mild facial dysmorphism include upslanted palpebral fissures and prominent nasal bridge.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401910014	A rare, genetic, syndromic intellectual disability characterised by developmental delay, mild to moderate intellectual disability, low birth weight, moderate to severe short stature, microcephaly and variable hypergonadotropic hypogonadism. Mild facial dysmorphism include upslanted palpebral fissures and prominent nasal bridge.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core