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56852002: Achromatopsia (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\Anomaly of eye\Degenerative disorder of eye\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Cone dystrophy\Achromatopsia
\Finding of head region\Disorder of eye region\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Congenital anomaly of posterior segment of eye\Congenital anomaly of retina\Achromatopsia
\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\Achromatopsia
\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\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Cone dystrophy\Achromatopsia
\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\Congenital anomaly of retina\Achromatopsia
\Finding of head region\Disorder of eye region\Disorder of eye proper\Disorder of posterior segment of eye\Congenital anomaly of posterior segment of eye\Congenital anomaly of retina\Achromatopsia
\Finding of head region\Globe finding\Retina finding\Retinal disorder\Color blindness\Congenital color blindness\Achromatopsia
\Finding of head region\Globe finding\Retina finding\Retinal disorder\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Cone dystrophy\Achromatopsia
\Finding of head region\Globe finding\Retina finding\Retinal disorder\Congenital anomaly of retina\Achromatopsia
\Finding of head region\Globe finding\Disorder of eye proper\Anomaly of eye\Degenerative disorder of eye\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Cone dystrophy\Achromatopsia
\Finding of head region\Globe finding\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Congenital anomaly of posterior segment of eye\Congenital anomaly of retina\Achromatopsia
\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\Achromatopsia
\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\Degeneration of retina\Retinal dystrophy\Hereditary retinal dystrophy\Cone dystrophy\Achromatopsia
\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\Congenital anomaly of retina\Achromatopsia
\Finding of head region\Globe finding\Disorder of eye proper\Disorder of posterior segment of eye\Congenital anomaly of posterior segment of eye\Congenital anomaly of retina\Achromatopsia

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

94543012 Achromatopsia en Synonym Active Entire term case insensitive SNOMED CT core module

94544018 Monochromatism en Synonym Active Entire term case insensitive SNOMED CT core module

94546016 Achromatism en Synonym Active Entire term case insensitive SNOMED CT core module

795410010 Achromatopsia (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
Achromatopsia	Is a	Congenital color blindness	true	Inferred relationship	Existential restriction modifier
Achromatopsia	Is a	Hereditary retinal dystrophy	false	Inferred relationship	Existential restriction modifier
Achromatopsia	Is a	Hereditary disorder of the visual system	false	Inferred relationship	Existential restriction modifier
Achromatopsia	Finding site	Retinal structure	false	Inferred relationship	Existential restriction modifier
Achromatopsia	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Achromatopsia	Has interpretation	Abnormal	false	Inferred relationship	Existential restriction modifier	1
Achromatopsia	Interprets	Vision observable	false	Inferred relationship	Existential restriction modifier	1
Achromatopsia	Interprets	Visual function	false	Inferred relationship	Existential restriction modifier	1
Achromatopsia	Has interpretation	Abnormal	false	Inferred relationship	Existential restriction modifier	1
Achromatopsia	Interprets	Visual function	false	Inferred relationship	Existential restriction modifier	1
Achromatopsia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Achromatopsia	Finding site	Retinal structure	false	Inferred relationship	Existential restriction modifier	1
Achromatopsia	Associated morphology	Dystrophy	false	Inferred relationship	Existential restriction modifier	2
Achromatopsia	Finding site	Retinal structure	false	Inferred relationship	Existential restriction modifier	2
Achromatopsia	Is a	Congenital anomaly of retina	true	Inferred relationship	Existential restriction modifier
Achromatopsia	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Achromatopsia	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Achromatopsia	Is a	Cone dystrophy	true	Inferred relationship	Existential restriction modifier
Achromatopsia	Finding site	Cone of retina	true	Inferred relationship	Existential restriction modifier	1
Achromatopsia	Associated morphology	Dystrophy	true	Inferred relationship	Existential restriction modifier	1
Achromatopsia	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Rod monochromatism	Is a	False	Achromatopsia	Inferred relationship	Existential restriction modifier
Cone monochromatism	Is a	False	Achromatopsia	Inferred relationship	Existential restriction modifier
Complete achromatopsia	Is a	True	Achromatopsia	Inferred relationship	Existential restriction modifier
Incomplete achromatopsia	Is a	True	Achromatopsia	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
94543012	Achromatopsia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
94544018	Monochromatism	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
94546016	Achromatism	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
795410010	Achromatopsia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module