Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Dec 2022. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5159427015 | Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
5159428013 | Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome | Is a | Global developmental delay | true | Inferred relationship | Existential restriction modifier | ||
Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome | Is a | Disorder of digestive system specific to fetus OR newborn | true | Inferred relationship | Existential restriction modifier | ||
Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome | Is a | Genetic disease | true | Inferred relationship | Existential restriction modifier | ||
Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome | Is a | Congenital cataract | true | Inferred relationship | Existential restriction modifier | ||
Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome | Finding site | Structure of lens of eye | true | Inferred relationship | Existential restriction modifier | 1 | |
Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome | Associated morphology | Abnormally opaque structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome | Occurrence | Neonatal | true | Inferred relationship | Existential restriction modifier | 2 | |
Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome | Finding site | Liver structure | true | Inferred relationship | Existential restriction modifier | 2 | |
Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome | Is a | Neonatal disorder | true | Inferred relationship | Existential restriction modifier | ||
Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome | Is a | Hepatic failure | true | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets