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778008009: Fibroblast growth factor receptor 2-related bent bone dysplasia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3736398017 Perinatal lethal bent bone dysplasia en Synonym Active Entire term case insensitive SNOMED CT core module
3736399013 Fibroblast growth factor receptor 2-related bent bone dysplasia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3736400018 Fibroblast growth factor receptor 2-related bent bone dysplasia en Synonym Active Entire term case insensitive SNOMED CT core module
3736401019 FGFR2-related bent bone dysplasia en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fibroblast growth factor receptor 2-related bent bone dysplasia Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Fibroblast growth factor receptor 2-related bent bone dysplasia Is a Congenital anomaly of bone and joint true Inferred relationship Existential restriction modifier
Fibroblast growth factor receptor 2-related bent bone dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Fibroblast growth factor receptor 2-related bent bone dysplasia Is a Craniosynostosis syndrome true Inferred relationship Existential restriction modifier
Fibroblast growth factor receptor 2-related bent bone dysplasia Is a Bent bone dysplasia group true Inferred relationship Existential restriction modifier
Fibroblast growth factor receptor 2-related bent bone dysplasia Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Fibroblast growth factor receptor 2-related bent bone dysplasia Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Fibroblast growth factor receptor 2-related bent bone dysplasia Finding site Joint structure of suture of skull true Inferred relationship Existential restriction modifier 2
Fibroblast growth factor receptor 2-related bent bone dysplasia Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Fibroblast growth factor receptor 2-related bent bone dysplasia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Fibroblast growth factor receptor 2-related bent bone dysplasia Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Fibroblast growth factor receptor 2-related bent bone dysplasia Associated morphology Congenital premature fusion true Inferred relationship Existential restriction modifier 2
Fibroblast growth factor receptor 2-related bent bone dysplasia Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Fibroblast growth factor receptor 2-related bent bone dysplasia Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier
Fibroblast growth factor receptor 2-related bent bone dysplasia Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Fibroblast growth factor receptor 2-related bent bone dysplasia Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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