FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

715724002: 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:

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
5401053012 A rare non-syndromic syndactyly characterized by a distinctive combination of syndactyly and polydactyly, generally affecting the 3rd and 4th fingers and the 4th and 5th toes, bilaterally, with partial or complete reduplication of a digital ray within the syndactylous web. Additional features include 5th finger clinodactyly, camptodactyly and/or brachydactyly. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401054018 A rare non-syndromic syndactyly characterised by a distinctive combination of syndactyly and polydactyly, generally affecting the 3rd and 4th fingers and the 4th and 5th toes, bilaterally, with partial or complete reduplication of a digital ray within the syndactylous web. Additional features include 5th finger clinodactyly, camptodactyly and/or brachydactyly. 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 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 Congenital abnormal fusion 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

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start