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440350001: Fibroblast growth factor receptor 3-related craniosynostosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2789776013 Fibroblast growth factor receptor 3-related craniosynostosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2792566012 Fibroblast growth factor receptor 3-related craniosynostosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2792567015 Muenke syndrome en Synonym (core metadata concept) Inactive Entire term case insensitive (core metadata concept) SNOMED CT core
2794177011 Fibroblast growth factor receptor 3 (FGFR3) related craniosynostosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) est un(e) (attribut) anomalie congénitale du crâne (trouble) false Inferred relationship Some
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) localisation d'une constatation (attribut) Joint structure of suture of skull true Inferred relationship Some 1
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) est un(e) (attribut) syndrome de craniosynostose (trouble) true Inferred relationship Some
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) survenue (attribut) congénital false Inferred relationship Some
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) morphologie associée (attribut) Congenital premature fusion false Inferred relationship Some 1
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) localisation d'une constatation (attribut) Structure of coronal suture of skull false Inferred relationship Some 1
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) localisation d'une constatation (attribut) Structure of coronal suture of skull false Inferred relationship Some 1
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) morphologie associée (attribut) Congenital premature fusion true Inferred relationship Some 1
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) survenue (attribut) congénital false Inferred relationship Some 2
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) est un(e) (attribut) Congenital anomaly of bone and joint false Inferred relationship Some
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) est un(e) (attribut) Cranial suture finding false Inferred relationship Some
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) est un(e) (attribut) Disorder of skull (disorder) false Inferred relationship Some
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) est un(e) (attribut) Disorder of bone development (disorder) false Inferred relationship Some
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) morphologie associée (attribut) Congenital premature fusion false Inferred relationship Some 2
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) localisation d'une constatation (attribut) Joint structure of suture of skull false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Muenke syndrome est un(e) (attribut) True Fibroblast growth factor receptor 3-related craniosynostosis (disorder) Inferred relationship Some
Crouzon syndrome with acanthosis nigricans (disorder) est un(e) (attribut) True Fibroblast growth factor receptor 3-related craniosynostosis (disorder) Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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