FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

715725001: Syndactyly type 3 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core
3303527016 Syndactyly type 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303528014 Syndactyly of fingers 4 and 5 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

Back to Start