4602007: Robin sequence (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation à propos d'une région de la tête et du cou\Head finding (finding)\...

\Finding of head region\Finding of face\Disorder of face (disorder)\Congenital anomaly of face (disorder)\Multiple malformation syndrome with facial defects as major feature\Robin sequence (disorder)

\affection de la tête\Disorder of face (disorder)\Congenital anomaly of face (disorder)\Multiple malformation syndrome with facial defects as major feature\Robin sequence (disorder)
\affection de la tête\Congenital anomaly of head\Congenital anomaly of face (disorder)\Multiple malformation syndrome with facial defects as major feature\Robin sequence (disorder)

\Disease\affection de la tête\Disorder of face (disorder)\Congenital anomaly of face (disorder)\Multiple malformation syndrome with facial defects as major feature\Robin sequence (disorder)
\Disease\affection de la tête\Congenital anomaly of head\Congenital anomaly of face (disorder)\Multiple malformation syndrome with facial defects as major feature\Robin sequence (disorder)
\Disease\Congenital disease\Congenital malformation\Congenital malformation syndrome (disorder)\syndrome de malformations multisystémiques\Multiple malformation syndrome with facial defects as major feature\Robin sequence (disorder)
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face (disorder)\Multiple malformation syndrome with facial defects as major feature\Robin sequence (disorder)
\Disease\trouble du développement\Congenital malformation\Congenital malformation syndrome (disorder)\syndrome de malformations multisystémiques\Multiple malformation syndrome with facial defects as major feature\Robin sequence (disorder)
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face (disorder)\Multiple malformation syndrome with facial defects as major feature\Robin sequence (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

1230294017 Pierre Robin association en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

783324010 Robin sequence (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

7920012 Robin sequence en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

7921011 Micrognathia-glossoptosis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

7922016 Pierre Robin syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Robin sequence (disorder)	morphologie associée (attribut)	structure anormale sur le plan morphologique	true	Inferred relationship	Some	1
Robin sequence (disorder)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Robin sequence (disorder)	est un(e) (attribut)	Multisystem disorder O-P (navigational concept)	false	Inferred relationship	Some
Robin sequence (disorder)	est un(e) (attribut)	Multiple malformation syndrome with facial defects as major feature	true	Inferred relationship	Some
Robin sequence (disorder)	morphologie associée (attribut)	Congenital malformation	false	Inferred relationship	Some
Robin sequence (disorder)	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Robin sequence (disorder)	morphologie associée (attribut)	Developmental abnormality	false	Inferred relationship	Some	1
Robin sequence (disorder)	localisation d'une constatation (attribut)	face	true	Inferred relationship	Some	1
Robin sequence (disorder)	survenue (attribut)	congénital	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Joint contractures, developmental delay, Pierre Robin syndrome (disorder)	est un(e) (attribut)	True	Robin sequence (disorder)	Inferred relationship	Some
Ventricular extrasystoles with syncope, perodactyly and Robin sequence syndrome (disorder)	est un(e) (attribut)	True	Robin sequence (disorder)	Inferred relationship	Some
Pierre Robin sequence faciodigital anomaly syndrome (disorder)	est un(e) (attribut)	True	Robin sequence (disorder)	Inferred relationship	Some
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome (disorder)	est un(e) (attribut)	True	Robin sequence (disorder)	Inferred relationship	Some
Intellectual disability, brachydactyly, Pierre Robin syndrome (disorder)	est un(e) (attribut)	True	Robin sequence (disorder)	Inferred relationship	Some
syndrome de séquence de Robin-oligodactylie	est un(e) (attribut)	True	Robin sequence (disorder)	Inferred relationship	Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)