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724000006: Retinohepatoendocrinologic syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3481792012 Retinohepatoendocrinologic syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3481793019 Retinohepatoendocrinologic syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3481794013 RHE (retinohepatoendocrinologic) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3481795014 RHE syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinohepatoendocrinologic syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Retinohepatoendocrinologic syndrome Is a Disorder of liver true Inferred relationship Existential restriction modifier
Retinohepatoendocrinologic syndrome Is a Cone dystrophy true Inferred relationship Existential restriction modifier
Retinohepatoendocrinologic syndrome Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Retinohepatoendocrinologic syndrome Is a Hereditary disorder of endocrine system true Inferred relationship Existential restriction modifier
Retinohepatoendocrinologic syndrome Associated morphology Degeneration false Inferred relationship Existential restriction modifier 3
Retinohepatoendocrinologic syndrome Finding site Liver structure false Inferred relationship Existential restriction modifier 3
Retinohepatoendocrinologic syndrome Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 4
Retinohepatoendocrinologic syndrome Finding site Retinal structure false Inferred relationship Existential restriction modifier 4
Retinohepatoendocrinologic syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Retinohepatoendocrinologic syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Retinohepatoendocrinologic syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Retinohepatoendocrinologic syndrome Finding site Structure of endocrine system false Inferred relationship Existential restriction modifier 5
Retinohepatoendocrinologic syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Retinohepatoendocrinologic syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Retinohepatoendocrinologic syndrome Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Retinohepatoendocrinologic syndrome Finding site Liver structure true Inferred relationship Existential restriction modifier 1
Retinohepatoendocrinologic syndrome Finding site Cone of retina true Inferred relationship Existential restriction modifier 2
Retinohepatoendocrinologic syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 2
Retinohepatoendocrinologic syndrome Finding site Structure of endocrine system true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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