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720953006: Fibular dimelia diplopodia syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3322626019 Leg duplication mirror foot syndrome en Synonym Active Case insensitive SNOMED CT core
3322628018 Fibular dimelia diplopodia syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3322629014 Fibular dimelia diplopodia syndrome en Synonym Active Case insensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fibular dimelia diplopodia syndrome Occurrence Congenital true Inferred relationship Some 1
Fibular dimelia diplopodia syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Fibular dimelia diplopodia syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Fibular dimelia diplopodia syndrome Finding site Bone structure of fibula true Inferred relationship Some 1
Fibular dimelia diplopodia syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Fibular dimelia diplopodia syndrome Associated morphology Double structure true Inferred relationship Some 1
Fibular dimelia diplopodia syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
Fibular dimelia diplopodia syndrome Is a Duplication of fibula true Inferred relationship Some
Fibular dimelia diplopodia syndrome Is a Congenital anomaly of foot true Inferred relationship Some
Fibular dimelia diplopodia syndrome Occurrence Congenital true Inferred relationship Some 2
Fibular dimelia diplopodia syndrome Occurrence Congenital false Inferred relationship Some 3
Fibular dimelia diplopodia syndrome Associated morphology Developmental abnormality false Inferred relationship Some 2
Fibular dimelia diplopodia syndrome Finding site Foot structure true Inferred relationship Some 2
Fibular dimelia diplopodia syndrome Associated morphology Double structure false Inferred relationship Some 3
Fibular dimelia diplopodia syndrome Finding site Bone structure of fibula false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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