FHIR © HL7.org | Server Home | FHIR Server FHIR Server 4.0.1 | FHIR Version n/a User: [n/a]

232148006: Congenital color blindness (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
\Finding of head region\Globe finding\Retina finding\Retinal disorder\Color blindness\Congenital color blindness
\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

\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

\Eye / vision finding\Globe finding\Retina finding\Retinal disorder\Color blindness\Congenital color blindness
\Eye / vision finding\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
\Eye / vision finding\Visual system disorder\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
\Eye / vision finding\Visual system disorder\Disorder of vision\Color vision deficiency\Congenital color blindness
\Eye / vision finding\Visual system disorder\Disorder of vision\Visual disturbance\Color blindness\Congenital color blindness

\Disease\Disorder of body system\Visual system disorder\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
\Disease\Disorder of body system\Visual system disorder\Disorder of vision\Color vision deficiency\Congenital color blindness
\Disease\Disorder of body system\Visual system disorder\Disorder of vision\Visual disturbance\Color blindness\Congenital color blindness
\Disease\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
\Disease\Congenital disease\Congenital color blindness

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

347840013 Congenital color blindness en Synonym Active Entire term case insensitive SNOMED CT core module
347841012 Congenital colour blindness en Synonym Active Entire term case insensitive SNOMED CT core module
620175012 Congenital color blindness (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital color blindness	Is a	Color vision deficiency	true	Inferred relationship	Existential restriction modifier
Congenital color blindness	Is a	Color blindness	true	Inferred relationship	Existential restriction modifier
Congenital color blindness	Finding site	Retinal structure	false	Inferred relationship	Existential restriction modifier
Congenital color blindness	Is a	Congenital anomaly of eye	false	Inferred relationship	Existential restriction modifier
Congenital color blindness	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Congenital color blindness	Is a	Congenital disease	true	Inferred relationship	Existential restriction modifier
Congenital color blindness	Has interpretation	Abnormal	false	Inferred relationship	Existential restriction modifier	1
Congenital color blindness	Interprets	Vision observable	false	Inferred relationship	Existential restriction modifier	1
Congenital color blindness	Interprets	Visual function	false	Inferred relationship	Existential restriction modifier	1
Congenital color blindness	Has interpretation	Abnormal	false	Inferred relationship	Existential restriction modifier	1
Congenital color blindness	Interprets	Visual function	false	Inferred relationship	Existential restriction modifier	1
Congenital color blindness	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Congenital color blindness	Finding site	Retinal structure	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Protan defect	Is a	True	Congenital color blindness	Inferred relationship	Existential restriction modifier
Tritan defect	Is a	True	Congenital color blindness	Inferred relationship	Existential restriction modifier
Achromatopsia	Is a	True	Congenital color blindness	Inferred relationship	Existential restriction modifier
Deutan defect	Is a	True	Congenital color blindness	Inferred relationship	Existential restriction modifier
Blue cone monochromatism	Is a	True	Congenital color blindness	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
347840013	Congenital color blindness	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
347841012	Congenital colour blindness	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
620175012	Congenital color blindness (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module