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720953006: Fibular dimelia diplopodia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3322626019 Leg duplication mirror foot syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3322628018 Fibular dimelia diplopodia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3322629014 Fibular dimelia diplopodia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5402526015 A very rare, genetic, congenital limb malformation syndrome characterized by duplication of the fibula associated with pre-axial mirror polydactyly of the foot, that may occur as an isolated malformation or be associated with other anomalies, including ulnar dimelia, facial abnormalities and sacrococcygeal teratoma. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402527012 A very rare, genetic, congenital limb malformation syndrome characterised by duplication of the fibula associated with pre-axial mirror polydactyly of the foot, that may occur as an isolated malformation or be associated with other anomalies, including ulnar dimelia, facial abnormalities and sacrococcygeal teratoma. 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
Fibular dimelia diplopodia syndrome (disorder) Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
Fibular dimelia diplopodia syndrome (disorder) Is a Duplication of fibula true Inferred relationship Some
Fibular dimelia diplopodia syndrome (disorder) Is a Congenital abnormality of foot and toes (disorder) true Inferred relationship Some
Fibular dimelia diplopodia syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Fibular dimelia diplopodia syndrome (disorder) Occurrence Congenital false Inferred relationship Some 3
Fibular dimelia diplopodia syndrome (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 2
Fibular dimelia diplopodia syndrome (disorder) Finding site Foot structure true Inferred relationship Some 2
Fibular dimelia diplopodia syndrome (disorder) Associated morphology Double structure false Inferred relationship Some 3
Fibular dimelia diplopodia syndrome (disorder) Finding site Bone structure of fibula false Inferred relationship Some 3
Fibular dimelia diplopodia syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Fibular dimelia diplopodia syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Fibular dimelia diplopodia syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Fibular dimelia diplopodia syndrome (disorder) Finding site Bone structure of fibula true Inferred relationship Some 1
Fibular dimelia diplopodia syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Fibular dimelia diplopodia syndrome (disorder) Associated morphology Double structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

GB English

US English

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