715404000: syndrome améloonychohypohidrotique (trouble)

SNOMED CT Concept\constatation clinique\...

\Skin AND/OR mucosa finding (finding)\Skin finding\affection de la peau (trouble)\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\syndrome améloonychohypohidrotique

\constatation générale à propos des tissus mous\Skin finding\affection de la peau (trouble)\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\syndrome améloonychohypohidrotique
\constatation générale à propos des tissus mous\Disorder of soft tissue\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\syndrome améloonychohypohidrotique

\Integumentary system finding\troubles tégumentaires\Hereditary disorder of the integument\syndrome améloonychohypohidrotique
\Integumentary system finding\troubles tégumentaires\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\syndrome améloonychohypohidrotique
\Integumentary system finding\troubles tégumentaires\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\syndrome améloonychohypohidrotique
\Integumentary system finding\Skin finding\affection de la peau (trouble)\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\syndrome améloonychohypohidrotique

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of the integument\syndrome améloonychohypohidrotique
\Disease\Genetic disease\maladie héréditaire\Developmental hereditary disorder\syndrome améloonychohypohidrotique
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\syndrome améloonychohypohidrotique
\Disease\Disorder of embryonic structure (disorder)\Congenital ectodermal defect\Ectodermal dysplasia\syndrome améloonychohypohidrotique
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of the integument\syndrome améloonychohypohidrotique
\Disease\affection d'un système corporel\troubles tégumentaires\Hereditary disorder of the integument\syndrome améloonychohypohidrotique
\Disease\affection d'un système corporel\troubles tégumentaires\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\syndrome améloonychohypohidrotique
\Disease\affection d'un système corporel\troubles tégumentaires\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\syndrome améloonychohypohidrotique
\Disease\Congenital disease\Congenital malformation\Congenital ectodermal defect\Ectodermal dysplasia\syndrome améloonychohypohidrotique
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\syndrome améloonychohypohidrotique
\Disease\Disorder of soft tissue\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\syndrome améloonychohypohidrotique
\Disease\trouble du développement\Developmental hereditary disorder\syndrome améloonychohypohidrotique
\Disease\trouble du développement\Congenital malformation\Congenital ectodermal defect\Ectodermal dysplasia\syndrome améloonychohypohidrotique
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\syndrome améloonychohypohidrotique

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
syndrome améloonychohypohidrotique	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
syndrome améloonychohypohidrotique	survenue (attribut)	congénital	true	Inferred relationship	Some	1
syndrome améloonychohypohidrotique	localisation d'une constatation (attribut)	structure de la peau	true	Inferred relationship	Some	1
syndrome améloonychohypohidrotique	morphologie associée (attribut)	structure anormale sur le plan morphologique	true	Inferred relationship	Some	1
syndrome améloonychohypohidrotique	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	2
syndrome améloonychohypohidrotique	morphologie associée (attribut)	dysplasie	true	Inferred relationship	Some	2
syndrome améloonychohypohidrotique	est un(e) (attribut)	Developmental hereditary disorder	true	Inferred relationship	Some
syndrome améloonychohypohidrotique	est un(e) (attribut)	Ectodermal dysplasia	true	Inferred relationship	Some
syndrome améloonychohypohidrotique	est un(e) (attribut)	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
syndrome améloonychohypohidrotique	est un(e) (attribut)	Hereditary disorder of the integument	true	Inferred relationship	Some
syndrome améloonychohypohidrotique	survenue (attribut)	congénital	true	Inferred relationship	Some	2
syndrome améloonychohypohidrotique	survenue (attribut)	congénital	false	Inferred relationship	Some	3
syndrome améloonychohypohidrotique	morphologie associée (attribut)	Congenital dysplasia	false	Inferred relationship	Some	2
syndrome améloonychohypohidrotique	localisation d'une constatation (attribut)	Ectoderm structure	true	Inferred relationship	Some	2
syndrome améloonychohypohidrotique	morphologie associée (attribut)	Developmental abnormality	false	Inferred relationship	Some	3
syndrome améloonychohypohidrotique	localisation d'une constatation (attribut)	structure de la peau	false	Inferred relationship	Some	3

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
1009841000172114	syndrome améloonychohypohidrotique	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3302487013	Ameloonychohypohidrotic syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3302488015	Ameloonychohypohidrotic syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3302489011	Amelo-onycho-hypohidrotic syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
747451000241118	syndrome améloonychohypohidrotique (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3302490019	A rare syndrome comprising hypocalcified-hypoplastic tooth enamel, onycholysis with subungual hyperkeratosis, and hypohidrosis.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core