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723827003: syndrome de Grant (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3426288012 Grant syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3426289016 Grant syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
760001000241115 syndrome de Grant (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
913091000172115 syndrome de Grant fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3426287019 A rare osteogenesis imperfecta-like disorder, described in two patients to date, with clinical characteristics of persistent wormian bones, blue sclera, mandibular hypoplasia, shallow glenoid fossa, and campomelia. There have been no further descriptions in the literature since 1986. 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
Grant syndrome survenue (attribut) congénital true Inferred relationship Some 1
Grant syndrome localisation d'une constatation (attribut) structure osseuse true Inferred relationship Some 1
Grant syndrome morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 1
Grant syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Grant syndrome morphologie associée (attribut) dysplasie true Inferred relationship Some 1
Grant syndrome interprète (attribut) ostéodensitométrie true Inferred relationship Some 2
Grant syndrome a pour interprétation (attribut) au-dessus de l'étendue de référence true Inferred relationship Some 2
Grant syndrome est un(e) (attribut) Congenital anomaly of skeletal bone true Inferred relationship Some
Grant syndrome est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
Grant syndrome est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Grant syndrome est un(e) (attribut) Dysplasia with increased bone density true Inferred relationship Some
Grant syndrome est un(e) (attribut) Connective tissue hereditary disorder false Inferred relationship Some
Grant syndrome est un(e) (attribut) Hereditary disorder of musculoskeletal system true Inferred relationship Some
Grant syndrome morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 2
Grant syndrome survenue (attribut) congénital false Inferred relationship Some 2
Grant syndrome 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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