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716230005: Shprintzen Goldberg omphalocele syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3305151017 Shprintzen Goldberg omphalocele syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3305152012 Shprintzen Goldberg omphalocele syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3305153019 Omphalocele syndrome Shprintzen Goldberg type en Synonym Active Only initial character case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Shprintzen Goldberg omphalocele syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Shprintzen Goldberg omphalocele syndrome Is a Congenital omphalocele true Inferred relationship Existential restriction modifier
Shprintzen Goldberg omphalocele syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Shprintzen Goldberg omphalocele syndrome Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier
Shprintzen Goldberg omphalocele syndrome Associated morphology Hernial opening false Inferred relationship Existential restriction modifier 6
Shprintzen Goldberg omphalocele syndrome Finding site Abdominal wall structure false Inferred relationship Existential restriction modifier 6
Shprintzen Goldberg omphalocele syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 8
Shprintzen Goldberg omphalocele syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 8
Shprintzen Goldberg omphalocele syndrome Finding site Abdominal wall structure false Inferred relationship Existential restriction modifier 8
Shprintzen Goldberg omphalocele syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 10
Shprintzen Goldberg omphalocele syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 10
Shprintzen Goldberg omphalocele syndrome Finding site Face structure false Inferred relationship Existential restriction modifier 10
Shprintzen Goldberg omphalocele syndrome Associated morphology Herniated structure false Inferred relationship Existential restriction modifier 7
Shprintzen Goldberg omphalocele syndrome Finding site Abdominopelvic cavity structure false Inferred relationship Existential restriction modifier 7
Shprintzen Goldberg omphalocele syndrome Associated morphology Congenital protrusion false Inferred relationship Existential restriction modifier 9
Shprintzen Goldberg omphalocele syndrome Associated morphology Herniated structure false Inferred relationship Existential restriction modifier 9
Shprintzen Goldberg omphalocele syndrome Finding site Intestinal structure false Inferred relationship Existential restriction modifier 9
Shprintzen Goldberg omphalocele syndrome Associated morphology Congenital failure of fusion false Inferred relationship Existential restriction modifier 11
Shprintzen Goldberg omphalocele syndrome Associated morphology Hernial opening false Inferred relationship Existential restriction modifier 11
Shprintzen Goldberg omphalocele syndrome Finding site Umbilical structure false Inferred relationship Existential restriction modifier 11
Shprintzen Goldberg omphalocele syndrome Associated morphology Hernial opening false Inferred relationship Existential restriction modifier 1
Shprintzen Goldberg omphalocele syndrome Finding site Umbilical structure false Inferred relationship Existential restriction modifier 1
Shprintzen Goldberg omphalocele syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Shprintzen Goldberg omphalocele syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Shprintzen Goldberg omphalocele syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Shprintzen Goldberg omphalocele syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Shprintzen Goldberg omphalocele syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 1
Shprintzen Goldberg omphalocele syndrome Associated morphology Herniated structure true Inferred relationship Existential restriction modifier 3
Shprintzen Goldberg omphalocele syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Shprintzen Goldberg omphalocele syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Shprintzen Goldberg omphalocele syndrome Associated morphology Hernial opening true Inferred relationship Existential restriction modifier 2
Shprintzen Goldberg omphalocele syndrome Finding site Structure of abdominopelvic viscus false Inferred relationship Existential restriction modifier 3
Shprintzen Goldberg omphalocele syndrome Finding site Umbilical structure true Inferred relationship Existential restriction modifier 2
Shprintzen Goldberg omphalocele syndrome Finding site Structure of organ within abdominopelvic cavity false Inferred relationship Existential restriction modifier 3
Shprintzen Goldberg omphalocele syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Shprintzen Goldberg omphalocele syndrome Finding site Structure of abdominopelvic cavity and/or content true Inferred relationship Existential restriction modifier 3
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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