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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
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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