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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
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
929001000172115 syndrome d'Eiken fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
982031000172111 syndroom van Eiken nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
995021000172115 Eiken-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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