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

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

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 SNOMED CT core module
2792566012 Fibroblast growth factor receptor 3-related craniosynostosis en Synonym Active Entire term case insensitive SNOMED CT core module
2792567015 Muenke syndrome en Synonym Inactive Entire term case insensitive SNOMED CT core module
2794177011 Fibroblast growth factor receptor 3 (FGFR3) related craniosynostosis en Synonym Active Only initial character case insensitive SNOMED CT core module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fibroblast growth factor receptor 3-related craniosynostosis Is a Craniosynostosis syndrome true Inferred relationship Existential restriction modifier
Fibroblast growth factor receptor 3-related craniosynostosis Occurrence Congenital false Inferred relationship Existential restriction modifier
Fibroblast growth factor receptor 3-related craniosynostosis Associated morphology Congenital premature fusion false Inferred relationship Existential restriction modifier 1
Fibroblast growth factor receptor 3-related craniosynostosis Finding site Structure of coronal suture of skull false Inferred relationship Existential restriction modifier 1
Fibroblast growth factor receptor 3-related craniosynostosis Finding site Structure of coronal suture of skull false Inferred relationship Existential restriction modifier 1
Fibroblast growth factor receptor 3-related craniosynostosis Associated morphology Congenital premature fusion true Inferred relationship Existential restriction modifier 1
Fibroblast growth factor receptor 3-related craniosynostosis Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Fibroblast growth factor receptor 3-related craniosynostosis Is a Congenital anomaly of bone and joint false Inferred relationship Existential restriction modifier
Fibroblast growth factor receptor 3-related craniosynostosis Is a Cranial suture finding false Inferred relationship Existential restriction modifier
Fibroblast growth factor receptor 3-related craniosynostosis Is a Disorder of skull false Inferred relationship Existential restriction modifier
Fibroblast growth factor receptor 3-related craniosynostosis Is a Disorder of bone development false Inferred relationship Existential restriction modifier
Fibroblast growth factor receptor 3-related craniosynostosis Associated morphology Congenital premature fusion false Inferred relationship Existential restriction modifier 2
Fibroblast growth factor receptor 3-related craniosynostosis Finding site Joint structure of suture of skull false Inferred relationship Existential restriction modifier 2
Fibroblast growth factor receptor 3-related craniosynostosis Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Fibroblast growth factor receptor 3-related craniosynostosis Is a Congenital anomaly of skull false Inferred relationship Existential restriction modifier
Fibroblast growth factor receptor 3-related craniosynostosis Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Fibroblast growth factor receptor 3-related craniosynostosis Finding site Joint structure of suture of skull true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Muenke syndrome Is a True Fibroblast growth factor receptor 3-related craniosynostosis Inferred relationship Existential restriction modifier
Crouzon syndrome with acanthosis nigricans Is a True Fibroblast growth factor receptor 3-related craniosynostosis Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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