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715532007: Weismann Netter syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3302945017 Weismann Netter syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3302947013 Weismann Netter syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3302948015 Anterior bowing of legs with dwarfism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302949011 An apparently familial disorder with features of anterior bowing of tibiae and fibulae and cortical hyperostosis on the concave side of the curvature. Associated anomalies may include short stature and in some cases mental retardation. 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
Weismann Netter syndrome (disorder) localisation d'une constatation (attribut) structure osseuse true Inferred relationship Some 1
Weismann Netter syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Weismann Netter syndrome (disorder) morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 1
Weismann Netter syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Weismann Netter syndrome (disorder) morphologie associée (attribut) dysplasie true Inferred relationship Some 1
Weismann Netter syndrome (disorder) est un(e) (attribut) Bent bone dysplasia group true Inferred relationship Some
Weismann Netter syndrome (disorder) morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 2
Weismann Netter syndrome (disorder) survenue (attribut) congénital false Inferred relationship Some 2
Weismann Netter syndrome (disorder) localisation d'une constatation (attribut) structure osseuse false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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