51445007: Protan defect (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of head and neck region\Head finding\...

\Finding of head region\Disorder of eye region\Disorder of eye proper\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina\Retinal disorder\Color blindness\Congenital color blindness\Protan defect
\Finding of head region\Globe finding\Retina finding\Retinal disorder\Color blindness\Congenital color blindness\Protan defect
\Finding of head region\Globe finding\Disorder of eye proper\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina\Retinal disorder\Color blindness\Congenital color blindness\Protan defect

\Disorder of head\Disorder of eye region\Disorder of eye proper\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina\Retinal disorder\Color blindness\Congenital color blindness\Protan defect

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

85680019 Protan defect en Synonym Active Entire term case sensitive SNOMED CT core module

85681015 Protanomaly en Synonym Active Entire term case insensitive SNOMED CT core module

85682010 Protanopia en Synonym Active Entire term case insensitive SNOMED CT core module

789345011 Protan defect (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Protan defect	Is a	Congenital color blindness	true	Inferred relationship	Existential restriction modifier
Protan defect	Finding site	Retinal structure	false	Inferred relationship	Existential restriction modifier
Protan defect	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Protan defect	Has interpretation	Abnormal	false	Inferred relationship	Existential restriction modifier	1
Protan defect	Interprets	Vision observable	false	Inferred relationship	Existential restriction modifier	1
Protan defect	Interprets	Visual function	false	Inferred relationship	Existential restriction modifier	1
Protan defect	Has interpretation	Abnormal	false	Inferred relationship	Existential restriction modifier	1
Protan defect	Interprets	Visual function	false	Inferred relationship	Existential restriction modifier	1
Protan defect	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Protan defect	Finding site	Retinal structure	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets