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720863002: Eiken 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
3322339011 Eiken syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3322340013 Eiken syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402516010 A rare, genetic, primary bone dysplasia syndrome characterized by multiple epiphyseal dysplasia, severely delayed ossification (mainly of the epiphyses, pubic symphysis, hands and feet), abnormal modeling of the bones in hands and feet, abnormal pelvis cartilage persistence, and mild growth retardation. Calcium, phosphate and vitamin D serum levels are typically within normal range, while parathyroid hormone serum levels are normal to slightly elevated. Oligodontia has been rarely associated. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402517018 A rare, genetic, primary bone dysplasia syndrome characterised by multiple epiphyseal dysplasia, severely delayed ossification (mainly of the epiphyses, pubic symphysis, hands and feet), abnormal modelling of the bones in hands and feet, abnormal pelvis cartilage persistence, and mild growth retardation. Calcium, phosphate and vitamin D serum levels are typically within normal range, while parathyroid hormone serum levels are normal to slightly elevated. Oligodontia has been rarely associated. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3322339011 Eiken syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3322340013 Eiken syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3322341012 A rare familial skeletal dysplasia with characteristics of multiple epiphyseal dysplasia with extremely retarded ossification. It has been described in 6 members of a unique consanguineous family. A mutation in PTHR1 gene is responsible for this syndrome. Transmission is autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402516010 A rare, genetic, primary bone dysplasia syndrome characterized by multiple epiphyseal dysplasia, severely delayed ossification (mainly of the epiphyses, pubic symphysis, hands and feet), abnormal modeling of the bones in hands and feet, abnormal pelvis cartilage persistence, and mild growth retardation. Calcium, phosphate and vitamin D serum levels are typically within normal range, while parathyroid hormone serum levels are normal to slightly elevated. Oligodontia has been rarely associated. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402517018 A rare, genetic, primary bone dysplasia syndrome characterised by multiple epiphyseal dysplasia, severely delayed ossification (mainly of the epiphyses, pubic symphysis, hands and feet), abnormal modelling of the bones in hands and feet, abnormal pelvis cartilage persistence, and mild growth retardation. Calcium, phosphate and vitamin D serum levels are typically within normal range, while parathyroid hormone serum levels are normal to slightly elevated. Oligodontia has been rarely associated. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3389401001000119 Eiken-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
929001000172115 syndrome d'Eiken fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
929001000172115 syndrome d'Eiken fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3389401001000119 Eiken-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Eiken syndrome Is a Multiple epiphyseal dysplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Eiken syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Eiken syndrome Is a Osteopenia true Inferred relationship Existential restriction modifier (core metadata concept)
Eiken syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 4
Eiken syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
Eiken syndrome Finding site Structure of epiphysis false Inferred relationship Existential restriction modifier (core metadata concept) 4
Eiken syndrome Associated morphology Osteopenia false Inferred relationship Existential restriction modifier (core metadata concept) 3
Eiken syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Eiken syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Eiken syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Eiken syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Eiken syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Eiken syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Eiken syndrome Associated morphology Osteopenia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Eiken syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Eiken syndrome Finding site Structure of epiphysis true Inferred relationship Existential restriction modifier (core metadata concept) 1
Eiken syndrome Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Eiken syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Eiken syndrome Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 3
Eiken syndrome Interprets Height / growth measure (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Eiken syndrome Associated morphology Demineralized structure true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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