1186730002: Gabriele-de Vries syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Mental state, behaviour and/or psychosocial function finding\Behaviour finding\Intellectual disability\Gabriele-de Vries syndrome

\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\Gabriele-de Vries syndrome

\Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Gabriele-de Vries syndrome
\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Gabriele-de Vries syndrome

\Functional finding\Cognitive function finding\Impaired cognition\Intellectual disability\Gabriele-de Vries syndrome
\Functional finding\Cognitive function finding\Intellectual ability - finding\Intellectual disability\Gabriele-de Vries syndrome
\Functional finding\Intelligence finding\Intellectual ability - finding\Intellectual disability\Gabriele-de Vries syndrome

\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Gabriele-de Vries syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Gabriele-de Vries syndrome
\Disease\Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Gabriele-de Vries syndrome
\Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Gabriele-de Vries syndrome
\Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Gabriele-de Vries syndrome
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Gabriele-de Vries syndrome
\Disease\Developmental disorder\Neurodevelopmental disorder\Intellectual disability\Gabriele-de Vries syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Gabriele-de Vries syndrome
\Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Gabriele-de Vries syndrome
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Gabriele-de Vries syndrome

Status: current, Primitive. Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

4667487013 YY1 haploinsufficiency syndrome en Synonym Active Case sensitive SNOMED CT core

4667488015 Gabriele-de Vries syndrome en Synonym Active Case sensitive SNOMED CT core

4667489011 Gabriele-de Vries syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core

4667493017 A rare genetic multiple congenital anomalies/dysmorphic syndrome characterised by variable developmental delay and intellectual disability, movement disorder or gait abnormalities and dysmorphic craniofacial features (such as facial asymmetry, broad forehead, posteriorly rotated ears, thick lower lip, micrognathia, or cleft palate). A variety of congenital malformations have been reported in addition, including ocular, renal, cardiac and joint anomalies, among others. Some patients show behavioural alterations (autism, hyperactivity, or anxiety). en Definition Active Case sensitive SNOMED CT core

4667494011 A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by variable developmental delay and intellectual disability, movement disorder or gait abnormalities and dysmorphic craniofacial features (such as facial asymmetry, broad forehead, posteriorly rotated ears, thick lower lip, micrognathia, or cleft palate). A variety of congenital malformations have been reported in addition, including ocular, renal, cardiac and joint anomalies, among others. Some patients show behavioral alterations (autism, hyperactivity, or anxiety). en Definition Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Gabriele-de Vries syndrome	Is a	Intellectual disability	true	Inferred relationship	Some
Gabriele-de Vries syndrome	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Gabriele-de Vries syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Some
Gabriele-de Vries syndrome	Is a	Multiple malformation syndrome with facial defects as major feature	true	Inferred relationship	Some
Gabriele-de Vries syndrome	Occurrence	Congenital	true	Inferred relationship	Some	1
Gabriele-de Vries syndrome	Finding site	Face structure	true	Inferred relationship	Some	1
Gabriele-de Vries syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Some	1
Gabriele-de Vries syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1
Gabriele-de Vries syndrome	Interprets	Intellectual ability	true	Inferred relationship	Some	2
Gabriele-de Vries syndrome	Has interpretation	Impaired	true	Inferred relationship	Some	2
Gabriele-de Vries syndrome	Interprets	Adaptation behaviour	true	Inferred relationship	Some	3
Gabriele-de Vries syndrome	Has interpretation	Impaired	true	Inferred relationship	Some	3

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
4667487013	YY1 haploinsufficiency syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
4667488015	Gabriele-de Vries syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
4667489011	Gabriele-de Vries syndrome (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core
4667493017	A rare genetic multiple congenital anomalies/dysmorphic syndrome characterised by variable developmental delay and intellectual disability, movement disorder or gait abnormalities and dysmorphic craniofacial features (such as facial asymmetry, broad forehead, posteriorly rotated ears, thick lower lip, micrognathia, or cleft palate). A variety of congenital malformations have been reported in addition, including ocular, renal, cardiac and joint anomalies, among others. Some patients show behavioural alterations (autism, hyperactivity, or anxiety).	en	Definition	Active	Case sensitive	SNOMED CT core
4667494011	A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by variable developmental delay and intellectual disability, movement disorder or gait abnormalities and dysmorphic craniofacial features (such as facial asymmetry, broad forehead, posteriorly rotated ears, thick lower lip, micrognathia, or cleft palate). A variety of congenital malformations have been reported in addition, including ocular, renal, cardiac and joint anomalies, among others. Some patients show behavioral alterations (autism, hyperactivity, or anxiety).	en	Definition	Active	Case sensitive	SNOMED CT core