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770434009: Familial benign flecked retina (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
3700846017 Familial benign flecked retina en Synonym Active Entire term case insensitive SNOMED CT core module
3700847014 Familial benign flecked retina (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
Familial benign flecked retina Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Familial benign flecked retina Finding site Retinal structure true Inferred relationship Existential restriction modifier 1
Familial benign flecked retina Is a Hereditary retinal dystrophy true Inferred relationship Existential restriction modifier
Familial benign flecked retina Is a Retinal flecking true Inferred relationship Existential restriction modifier
Familial benign flecked retina Finding site Retinal structure true Inferred relationship Existential restriction modifier 2
Familial benign flecked retina Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Familial benign flecked retina Associated morphology Deposition true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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