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715725001: Syndactyly type 3 (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3303526013 Syndactyly type 3 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3303527016 Syndactyly type 3 en Synonym Active Case insensitive SNOMED CT core
3303528014 Syndactyly of fingers 4 and 5 en Synonym Active Case insensitive SNOMED CT core
3303529018 A rare congenital distal limb malformation with complete and bilateral syndactyly between the fourth and fifth fingers. In most cases, it is a soft tissue syndactyly, but occasionally the distal phalanges may be fused. The feet are not affected. Inherited in an autosomal dominant manner. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Syndactyly type 3 Pathological process Pathological developmental process true Inferred relationship Some 1
Syndactyly type 3 Is a Developmental hereditary disorder true Inferred relationship Some
Syndactyly type 3 Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Syndactyly type 3 Is a Syndactyly of fingers true Inferred relationship Some
Syndactyly type 3 Associated morphology Congenital abnormal fusion true Inferred relationship Some 1
Syndactyly type 3 Occurrence Congenital true Inferred relationship Some 1
Syndactyly type 3 Finding site Finger structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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