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1260140008: Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome (disorder)


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


0 descendants.

Expanded Value Set


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

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