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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
5155334011 A rare genetic primary bent bone dysplasia with characteristics of anterior diaphyseal bowing of the tibia and fibula, broadening of the fibula, posterior cortical thickening of both bones and short stature. Additional skeletal abnormalities include scoliosis with marked lumbar lordosis, horizontal sacrum and square iliac wings and/or, less frequently, vertebral malformations, abnormal shape of the clavicles and ribs, calvarial hyperostosis and delayed eruption of permanent teeth. Delayed ambulation is also frequently associated. 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) Is a Bent bone dysplasia group true Inferred relationship Some
Weismann Netter syndrome (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 2
Weismann Netter syndrome (disorder) Occurrence Congenital false Inferred relationship Some 2
Weismann Netter syndrome (disorder) Finding site Bone structure false Inferred relationship Some 2
Weismann Netter syndrome (disorder) Finding site Bone structure true Inferred relationship Some 1
Weismann Netter syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Weismann Netter syndrome (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 1
Weismann Netter syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Weismann Netter syndrome (disorder) Associated morphology Dysplasia true Inferred relationship Some 1
Weismann Netter syndrome (disorder) Is a Genetic disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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