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28835009: Retinitis pigmentosa (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation à propos d'une région de la tête et du cou\Head finding (finding)\...

\Finding of head region\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\affection dégénérative de l'œil\dégénérescence de la rétine\Retinal dystrophy\Hereditary retinal dystrophy\rétinite pigmentaire (trouble)
\Finding of head region\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\trouble rétinien (trouble)\dégénérescence de la rétine\Retinal dystrophy\Hereditary retinal dystrophy\rétinite pigmentaire (trouble)
\Finding of head region\constatation à propos d'un globe oculaire\Retina finding (finding)\trouble rétinien (trouble)\dégénérescence de la rétine\Retinal dystrophy\Hereditary retinal dystrophy\rétinite pigmentaire (trouble)
\Finding of head region\constatation à propos d'un globe oculaire\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\affection dégénérative de l'œil\dégénérescence de la rétine\Retinal dystrophy\Hereditary retinal dystrophy\rétinite pigmentaire (trouble)
\Finding of head region\constatation à propos d'un globe oculaire\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\trouble rétinien (trouble)\dégénérescence de la rétine\Retinal dystrophy\Hereditary retinal dystrophy\rétinite pigmentaire (trouble)

\affection de la tête\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\...

\Anomaly of eye (disorder)\affection dégénérative de l'œil\dégénérescence de la rétine\Retinal dystrophy\Hereditary retinal dystrophy\rétinite pigmentaire (trouble)

\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\trouble rétinien (trouble)\dégénérescence de la rétine\Retinal dystrophy\Hereditary retinal dystrophy\rétinite pigmentaire (trouble)

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of the visual system\Hereditary retinal dystrophy\rétinite pigmentaire (trouble)
\Disease\affection dégénérative\affection dégénérative de l'œil\dégénérescence de la rétine\Retinal dystrophy\Hereditary retinal dystrophy\rétinite pigmentaire (trouble)
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of the visual system\Hereditary retinal dystrophy\rétinite pigmentaire (trouble)
\Disease\affection d'un système corporel\affection du système visuel\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\affection dégénérative de l'œil\dégénérescence de la rétine\Retinal dystrophy\Hereditary retinal dystrophy\rétinite pigmentaire (trouble)
\Disease\affection d'un système corporel\affection du système visuel\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\trouble rétinien (trouble)\dégénérescence de la rétine\Retinal dystrophy\Hereditary retinal dystrophy\rétinite pigmentaire (trouble)
\Disease\affection d'un système corporel\affection du système visuel\Hereditary disorder of the visual system\Hereditary retinal dystrophy\rétinite pigmentaire (trouble)
\Disease\affection de la tête\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Anomaly of eye (disorder)\affection dégénérative de l'œil\dégénérescence de la rétine\Retinal dystrophy\Hereditary retinal dystrophy\rétinite pigmentaire (trouble)
\Disease\affection de la tête\Disorder of eye region (disorder)\Disorder of eye proper (disorder)\Disorder of posterior segment of eye\Disorder of vitreous body and/or retina (disorder)\trouble rétinien (trouble)\dégénérescence de la rétine\Retinal dystrophy\Hereditary retinal dystrophy\rétinite pigmentaire (trouble)

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
rétinite pigmentaire (trouble)	est un(e) (attribut)	Hereditary retinal dystrophy	true	Inferred relationship	Some
rétinite pigmentaire (trouble)	est un(e) (attribut)	Autosomal hereditary disorder	false	Inferred relationship	Some
rétinite pigmentaire (trouble)	morphologie associée (attribut)	Dystrophy (morphologic abnormality)	true	Inferred relationship	Some	1
rétinite pigmentaire (trouble)	localisation d'une constatation (attribut)	structure de la rétine	true	Inferred relationship	Some	1
rétinite pigmentaire (trouble)	localisation d'une constatation (attribut)	structure de la rétine	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder)	est un(e) (attribut)	True	rétinite pigmentaire (trouble)	Inferred relationship	Some
History of retinitis pigmentosa	constatation associée (attribut)	True	rétinite pigmentaire (trouble)	Inferred relationship	Some	1
syndrome associant rétinite pigmentaire et surdité	est un(e) (attribut)	False	rétinite pigmentaire (trouble)	Inferred relationship	Some
HSMN IV	est un(e) (attribut)	True	rétinite pigmentaire (trouble)	Inferred relationship	Some
Tapetoretinal dystrophy	est un(e) (attribut)	True	rétinite pigmentaire (trouble)	Inferred relationship	Some
Autosomal dominant retinitis pigmentosa	est un(e) (attribut)	True	rétinite pigmentaire (trouble)	Inferred relationship	Some
Autosomal recessive retinitis pigmentosa	est un(e) (attribut)	True	rétinite pigmentaire (trouble)	Inferred relationship	Some
X-linked retinitis pigmentosa	est un(e) (attribut)	True	rétinite pigmentaire (trouble)	Inferred relationship	Some
X-linked retinitis pigmentosa heterozygote	est un(e) (attribut)	False	rétinite pigmentaire (trouble)	Inferred relationship	Some
Family history of retinitis pigmentosa (situation)	constatation associée (attribut)	True	rétinite pigmentaire (trouble)	Inferred relationship	Some	1
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder)	est un(e) (attribut)	False	rétinite pigmentaire (trouble)	Inferred relationship	Some
Oculotrichodysplasia (disorder)	est un(e) (attribut)	False	rétinite pigmentaire (trouble)	Inferred relationship	Some
Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder)	est un(e) (attribut)	False	rétinite pigmentaire (trouble)	Inferred relationship	Some
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome	est un(e) (attribut)	True	rétinite pigmentaire (trouble)	Inferred relationship	Some

Reference Sets

Canada English language reference set (foundation metadata concept)

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1226074019	RP - Retinitis pigmentosa	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3397413010	Rétinite pigmentaire	fr	Synonym (core metadata concept)	Inactive	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
413421000241119	rétinite pigmentaire (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
48282015	Retinitis pigmentosa	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
614231000172113	rétinite pigmentaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
759560017	Retinitis pigmentosa (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core