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774152007: Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies (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
3728155011 Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies en Synonym Active Entire term case insensitive SNOMED CT core module
3728156012 Retinal dystrophy with inner nuclear layer and ganglion cell anomalies en Synonym Active Entire term case insensitive SNOMED CT core module
3728157015 Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies (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
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies Is a Hereditary retinal dystrophy true Inferred relationship Existential restriction modifier
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies Finding site Retinal structure true Inferred relationship Existential restriction modifier 1
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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