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770900000: Familial omphalocele syndrome with facial dysmorphism (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
3703339017 Familial omphalocele syndrome with facial dysmorphism (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3703340015 Familial omphalocele syndrome with facial dysmorphism en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial omphalocele syndrome with facial dysmorphism Is a Congenital anomaly of intestinal tract true Inferred relationship Existential restriction modifier
Familial omphalocele syndrome with facial dysmorphism Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Familial omphalocele syndrome with facial dysmorphism Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Familial omphalocele syndrome with facial dysmorphism Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Familial omphalocele syndrome with facial dysmorphism Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Familial omphalocele syndrome with facial dysmorphism Associated morphology Herniated structure true Inferred relationship Existential restriction modifier 4
Familial omphalocele syndrome with facial dysmorphism Is a Congenital omphalocele true Inferred relationship Existential restriction modifier
Familial omphalocele syndrome with facial dysmorphism Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Familial omphalocele syndrome with facial dysmorphism Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Familial omphalocele syndrome with facial dysmorphism Associated morphology Congenital protrusion false Inferred relationship Existential restriction modifier 1
Familial omphalocele syndrome with facial dysmorphism Finding site Intestinal structure true Inferred relationship Existential restriction modifier 1
Familial omphalocele syndrome with facial dysmorphism Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Familial omphalocele syndrome with facial dysmorphism Finding site Umbilical structure true Inferred relationship Existential restriction modifier 3
Familial omphalocele syndrome with facial dysmorphism Associated morphology Hernial opening true Inferred relationship Existential restriction modifier 3
Familial omphalocele syndrome with facial dysmorphism Finding site Face structure true Inferred relationship Existential restriction modifier 2
Familial omphalocele syndrome with facial dysmorphism Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Familial omphalocele syndrome with facial dysmorphism Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Familial omphalocele syndrome with facial dysmorphism Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Familial omphalocele syndrome with facial dysmorphism Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Familial omphalocele syndrome with facial dysmorphism Finding site Structure of abdominopelvic viscus false Inferred relationship Existential restriction modifier 4
Familial omphalocele syndrome with facial dysmorphism Associated morphology Protrusion true Inferred relationship Existential restriction modifier 1
Familial omphalocele syndrome with facial dysmorphism Finding site Structure of organ within abdominopelvic cavity false Inferred relationship Existential restriction modifier 4
Familial omphalocele syndrome with facial dysmorphism Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Familial omphalocele syndrome with facial dysmorphism Finding site Structure of abdominopelvic cavity and/or content true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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