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89392001: Prader-Willi syndrome (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation à propos du système nerveux central\constatation à propos l'encéphale\Disorder of brain (disorder)\Limbic disorder (disorder)\Disorder of hypothalamus (disorder)\affection de l'hypophyse (trouble)\Hypopituitarism\hypogonadisme hypogonadotrope (trouble)\Congenital hypogonadotropic hypogonadism (disorder)\Prader-Willi syndrome
\constatation à propos du système nerveux central\constatation à propos l'encéphale\Disorder of brain (disorder)\Limbic disorder (disorder)\Disorder of hypothalamus (disorder)\affection de l'hypophyse (trouble)\Disorder of anterior pituitary (disorder)\hypogonadisme hypogonadotrope (trouble)\Congenital hypogonadotropic hypogonadism (disorder)\Prader-Willi syndrome
\constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Limbic disorder (disorder)\Disorder of hypothalamus (disorder)\affection de l'hypophyse (trouble)\Hypopituitarism\hypogonadisme hypogonadotrope (trouble)\Congenital hypogonadotropic hypogonadism (disorder)\Prader-Willi syndrome
\constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Limbic disorder (disorder)\Disorder of hypothalamus (disorder)\affection de l'hypophyse (trouble)\Disorder of anterior pituitary (disorder)\hypogonadisme hypogonadotrope (trouble)\Congenital hypogonadotropic hypogonadism (disorder)\Prader-Willi syndrome

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

\constatation à propos l'encéphale\Disorder of brain (disorder)\Limbic disorder (disorder)\Disorder of hypothalamus (disorder)\affection de l'hypophyse (trouble)\...

\Hypopituitarism\hypogonadisme hypogonadotrope (trouble)\Congenital hypogonadotropic hypogonadism (disorder)\Prader-Willi syndrome

\Disorder of anterior pituitary (disorder)\hypogonadisme hypogonadotrope (trouble)\Congenital hypogonadotropic hypogonadism (disorder)\Prader-Willi syndrome

\affection de la tête\Disorder of brain (disorder)\Limbic disorder (disorder)\Disorder of hypothalamus (disorder)\affection de l'hypophyse (trouble)\...

\Hypopituitarism\hypogonadisme hypogonadotrope (trouble)\Congenital hypogonadotropic hypogonadism (disorder)\Prader-Willi syndrome

\Disorder of anterior pituitary (disorder)\hypogonadisme hypogonadotrope (trouble)\Congenital hypogonadotropic hypogonadism (disorder)\Prader-Willi syndrome

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
Prader-Willi syndrome	morphologie associée (attribut)	structure anormale sur le plan morphologique	true	Inferred relationship	Some	2
Prader-Willi syndrome	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	2
Prader-Willi syndrome	est un(e) (attribut)	Congenital hypogonadotropic hypogonadism (disorder)	true	Inferred relationship	Some
Prader-Willi syndrome	est un(e) (attribut)	Genetic disease	true	Inferred relationship	Some
Prader-Willi syndrome	est un(e) (attribut)	Neurodevelopmental disorder	true	Inferred relationship	Some
Prader-Willi syndrome	est un(e) (attribut)	syndrome de malformations multisystémiques	true	Inferred relationship	Some
Prader-Willi syndrome	survenue (attribut)	congénital	true	Inferred relationship	Some	3
Prader-Willi syndrome	localisation d'une constatation (attribut)	Structure of pars distalis of pituitary (body structure)	true	Inferred relationship	Some	3
Prader-Willi syndrome	localisation d'une constatation (attribut)	Gonadal endocrine structure	true	Inferred relationship	Some	1
Prader-Willi syndrome	morphologie associée (attribut)	Congenital malformation	false	Inferred relationship	Some
Prader-Willi syndrome	morphologie associée (attribut)	Congenital anomaly	false	Inferred relationship	Some	1
Prader-Willi syndrome	est un(e) (attribut)	Anomaly of chromosome pair 15	false	Inferred relationship	Some
Prader-Willi syndrome	est un(e) (attribut)	Multiple malformation syndrome with unusual brain and/or neuromuscular findings	false	Inferred relationship	Some
Prader-Willi syndrome	morphologie associée (attribut)	Congenital anomaly	false	Inferred relationship	Some	1
Prader-Willi syndrome	localisation d'une constatation (attribut)	Chromosome pair 15	false	Inferred relationship	Some	1
Prader-Willi syndrome	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Prader-Willi syndrome	localisation d'une constatation (attribut)	Chromosome pair 15	false	Inferred relationship	Some	1
Prader-Willi syndrome	survenue (attribut)	congénital	true	Inferred relationship	Some	2
Prader-Willi syndrome	morphologie associée (attribut)	Cellular AND/OR subcellular abnormality	false	Inferred relationship	Some	1
Prader-Willi syndrome	morphologie associée (attribut)	Developmental abnormality	false	Inferred relationship	Some	2
Prader-Willi syndrome	localisation d'une constatation (attribut)	Chromosome pair 15	false	Inferred relationship	Some	1
Prader-Willi syndrome	localisation d'une constatation (attribut)	Sex chromosome (cell structure)	false	Inferred relationship	Some
Prader-Willi syndrome	survenue (attribut)	congénital	false	Inferred relationship	Some
Prader-Willi syndrome	localisation d'une constatation (attribut)	structure de l'encéphale	false	Inferred relationship	Some	2
Prader-Willi syndrome	morphologie associée (attribut)	Alteration of chromosome structure	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Family history of Prader-Willi syndrome	constatation associée (attribut)	True	Prader-Willi syndrome	Inferred relationship	Some	1

Reference Sets

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)

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Id	Description	Lang	Type	Status	Case?	Module
148214012	Prader-Willi syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3793256012	Prader Labhart Willi syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
480471000241112	syndrome de Prader-Willi (trouble)	fr	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
832276019	Prader-Willi syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
935701000172117	syndrome de Prader-Labhart-Willi	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
980701000172116	syndrome de Prader-Willi	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)