715724002: syndactylie type 2 (aandoening)

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

\Finding of limb structure\Disorder of limb (disorder)\...

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

\Syndactyly (disorder)\Polysyndactyly (disorder)\Syndactyly type 2 (disorder)

\Polydactyly (disorder)\Polysyndactyly (disorder)\Syndactyly type 2 (disorder)

\Congenital anomaly of limb\Congenital anomaly of digit (disorder)\Syndactyly (disorder)\Polysyndactyly (disorder)\Syndactyly type 2 (disorder)
\Congenital anomaly of limb\Congenital anomaly of digit (disorder)\Polydactyly (disorder)\Polysyndactyly (disorder)\Syndactyly type 2 (disorder)
\Congenital anomaly of limb\Polymelia\Polydactyly (disorder)\Polysyndactyly (disorder)\Syndactyly type 2 (disorder)

\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Syndactyly type 2 (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Syndactyly type 2 (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of digit (disorder)\Syndactyly (disorder)\Polysyndactyly (disorder)\Syndactyly type 2 (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of digit (disorder)\Polydactyly (disorder)\Polysyndactyly (disorder)\Syndactyly type 2 (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of limb\Polymelia\Polydactyly (disorder)\Polysyndactyly (disorder)\Syndactyly type 2 (disorder)
\Disease\Disorder of limb (disorder)\Disorder of digit\Congenital anomaly of digit (disorder)\Syndactyly (disorder)\Polysyndactyly (disorder)\Syndactyly type 2 (disorder)
\Disease\Disorder of limb (disorder)\Disorder of digit\Congenital anomaly of digit (disorder)\Polydactyly (disorder)\Polysyndactyly (disorder)\Syndactyly type 2 (disorder)
\Disease\Disorder of limb (disorder)\Congenital anomaly of limb\Congenital anomaly of digit (disorder)\Syndactyly (disorder)\Polysyndactyly (disorder)\Syndactyly type 2 (disorder)
\Disease\Disorder of limb (disorder)\Congenital anomaly of limb\Congenital anomaly of digit (disorder)\Polydactyly (disorder)\Polysyndactyly (disorder)\Syndactyly type 2 (disorder)
\Disease\Disorder of limb (disorder)\Congenital anomaly of limb\Polymelia\Polydactyly (disorder)\Polysyndactyly (disorder)\Syndactyly type 2 (disorder)
\Disease\Developmental disorder\Developmental hereditary disorder\Syndactyly type 2 (disorder)
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of digit (disorder)\Syndactyly (disorder)\Polysyndactyly (disorder)\Syndactyly type 2 (disorder)
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of digit (disorder)\Polydactyly (disorder)\Polysyndactyly (disorder)\Syndactyly type 2 (disorder)
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of limb\Polymelia\Polydactyly (disorder)\Polysyndactyly (disorder)\Syndactyly type 2 (disorder)

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
Syndactyly type 2 (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Syndactyly type 2 (disorder)	Is a	Polydactyly (disorder)	false	Inferred relationship	Some
Syndactyly type 2 (disorder)	Is a	Syndactyly (disorder)	false	Inferred relationship	Some
Syndactyly type 2 (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	2
Syndactyly type 2 (disorder)	Finding site	Digit structure	true	Inferred relationship	Some	2
Syndactyly type 2 (disorder)	Occurrence	Congenital	false	Inferred relationship	Some	3
Syndactyly type 2 (disorder)	Finding site	Digit structure	false	Inferred relationship	Some	3
Syndactyly type 2 (disorder)	Associated morphology	congenitale afwijkende fusie	false	Inferred relationship	Some	2
Syndactyly type 2 (disorder)	Associated morphology	Supernumerary structure	false	Inferred relationship	Some	3
Syndactyly type 2 (disorder)	Is a	Polysyndactyly (disorder)	true	Inferred relationship	Some
Syndactyly type 2 (disorder)	Finding site	Digit structure	true	Inferred relationship	Some	1
Syndactyly type 2 (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Syndactyly type 2 (disorder)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Syndactyly type 2 (disorder)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	2
Syndactyly type 2 (disorder)	Associated morphology	Supernumerary structure	true	Inferred relationship	Some	1
Syndactyly type 2 (disorder)	Is a	Developmental hereditary disorder	true	Inferred relationship	Some
Syndactyly type 2 (disorder)	Associated morphology	Abnormally fused structure (morphologic abnormality)	true	Inferred relationship	Some	2

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
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
6394461000146115	syndactylie type 2	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6394471000146114	syndactylie type 2 (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6394481000146111	synpolydactylie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained 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