715724002: syndactylie type 2 (trouble)

SNOMED CT Concept\constatation clinique\...

\constatation à propos de la structure d'un membre\affection d'une extrémité\...

\Disorder of digit\Congenital anomaly of digit (disorder)\...

\Syndactyly (disorder)\polysyndactylie (trouble)\syndactylie type 2

\polydactylie\polysyndactylie (trouble)\syndactylie type 2

\Congenital anomaly of limb\Congenital anomaly of digit (disorder)\Syndactyly (disorder)\polysyndactylie (trouble)\syndactylie type 2
\Congenital anomaly of limb\Congenital anomaly of digit (disorder)\polydactylie\polysyndactylie (trouble)\syndactylie type 2
\Congenital anomaly of limb\Polymelia\polydactylie\polysyndactylie (trouble)\syndactylie type 2

\Disease\Genetic disease\maladie héréditaire\Developmental hereditary disorder\syndactylie type 2
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\syndactylie type 2
\Disease\affection d'une extrémité\Disorder of digit\Congenital anomaly of digit (disorder)\Syndactyly (disorder)\polysyndactylie (trouble)\syndactylie type 2
\Disease\affection d'une extrémité\Disorder of digit\Congenital anomaly of digit (disorder)\polydactylie\polysyndactylie (trouble)\syndactylie type 2
\Disease\affection d'une extrémité\Congenital anomaly of limb\Congenital anomaly of digit (disorder)\Syndactyly (disorder)\polysyndactylie (trouble)\syndactylie type 2
\Disease\affection d'une extrémité\Congenital anomaly of limb\Congenital anomaly of digit (disorder)\polydactylie\polysyndactylie (trouble)\syndactylie type 2
\Disease\affection d'une extrémité\Congenital anomaly of limb\Polymelia\polydactylie\polysyndactylie (trouble)\syndactylie type 2
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of digit (disorder)\Syndactyly (disorder)\polysyndactylie (trouble)\syndactylie type 2
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of digit (disorder)\polydactylie\polysyndactylie (trouble)\syndactylie type 2
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of limb\Polymelia\polydactylie\polysyndactylie (trouble)\syndactylie type 2
\Disease\trouble du développement\Developmental hereditary disorder\syndactylie type 2
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of digit (disorder)\Syndactyly (disorder)\polysyndactylie (trouble)\syndactylie type 2
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of digit (disorder)\polydactylie\polysyndactylie (trouble)\syndactylie type 2
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of limb\Polymelia\polydactylie\polysyndactylie (trouble)\syndactylie type 2

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
syndactylie type 2	localisation d'une constatation (attribut)	Digit structure	true	Inferred relationship	Some	1
syndactylie type 2	survenue (attribut)	congénital	true	Inferred relationship	Some	1
syndactylie type 2	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
syndactylie type 2	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	2
syndactylie type 2	morphologie associée (attribut)	Supernumerary structure	true	Inferred relationship	Some	1
syndactylie type 2	est un(e) (attribut)	Developmental hereditary disorder	true	Inferred relationship	Some
syndactylie type 2	est un(e) (attribut)	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
syndactylie type 2	est un(e) (attribut)	polydactylie	false	Inferred relationship	Some
syndactylie type 2	est un(e) (attribut)	Syndactyly (disorder)	false	Inferred relationship	Some
syndactylie type 2	survenue (attribut)	congénital	true	Inferred relationship	Some	2
syndactylie type 2	localisation d'une constatation (attribut)	Digit structure	true	Inferred relationship	Some	2
syndactylie type 2	survenue (attribut)	congénital	false	Inferred relationship	Some	3
syndactylie type 2	localisation d'une constatation (attribut)	Digit structure	false	Inferred relationship	Some	3
syndactylie type 2	morphologie associée (attribut)	Congenital abnormal fusion	true	Inferred relationship	Some	2
syndactylie type 2	morphologie associée (attribut)	Supernumerary structure	false	Inferred relationship	Some	3
syndactylie type 2	est un(e) (attribut)	polysyndactylie (trouble)	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
1000091000172118	syndactylie type 2	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3303522010	Syndactyly type 2 (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3303523017	Syndactyly type 2	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3303524011	Synpolydactyly	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
748361000241113	syndactylie type 2 (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
892591000172114	synpolydactylie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3303525012	A rare congenital distal limb malformation with the combination of syndactyly and polydactyly. In most cases affects the third and fourth fingers and the fourth and fifth toes bilaterally. Additional features include fifth finger clinodactyly, camptodactyly and/or brachydactyly. Inherited in an autosomal dominant manner.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core