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

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
3322627011 Fibular dimelia accompanied by complete tibial agenesis and mirror polydactyly or foot duplication is a rare developmental anomaly reported in at least 11 cases. It can be isolated or associated with ulnar dimelia, facial abnormalities and sacrococcygeal teratoma. The cause is unknown, but has been suggested that a teratogenic event occurs as developmental specification reaches the level of the future knee. A central role for the mesenchymal precursor, from which chondro-osseous morphology emerges, has also been suggested. Treatment is surgical and prosthesis is needed in order to improve the quality of life of affected children. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3905251000052116 syndrom med fibulär dimeli och diplopodi sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


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 utvecklingsabnormitet 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

GB English

US English

Back to Start