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702379005: Hypomyelination and congenital cataract (disorder)


Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2995368018 HCC - hypomyelination and congenital cataract en Synonym Active Case sensitive SNOMED CT core
2995422017 Hypomyelination and congenital cataract en Synonym Active Case insensitive SNOMED CT core
2995853012 Hypomyelination and congenital cataract (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypomyelination and congenital cataract Is a Hereditary disorder of nervous system true Inferred relationship Some
Hypomyelination and congenital cataract Is a Leukoencephalopathy true Inferred relationship Some
Hypomyelination and congenital cataract Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Hypomyelination and congenital cataract Finding site Cerebral white matter structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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