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763668009: syndrome de Lichtenstein (trouble)

Descriptions:

Id Description Lang Type Status Case? Module

3643231015 Lichtenstein syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3643232010 Lichtenstein syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

766301000241119 syndrome de Lichtenstein (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

975581000172116 syndrome de Lichtenstein fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

3643233017 Syndrome with characteristics of frequent infections associated with osteoporosis, a tendency for fractures and osseous anomalies. It has been described in two monozygotic twin brothers. Transmission is autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Lichtenstein syndrome	Pathological process (attribute)	Abnormal immune process (qualifier value)	true	Inferred relationship	Some	2
Lichtenstein syndrome	est un(e) (attribut)	Congenital immunodeficiency disease	true	Inferred relationship	Some
Lichtenstein syndrome	est un(e) (attribut)	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Lichtenstein syndrome	est un(e) (attribut)	Phagocytic cell dysfunction	true	Inferred relationship	Some
Lichtenstein syndrome	est un(e) (attribut)	Hereditary disorder of immune system	true	Inferred relationship	Some
Lichtenstein syndrome	est un(e) (attribut)	Disorder of immune structure (disorder)	true	Inferred relationship	Some
Lichtenstein syndrome	localisation d'une constatation (attribut)	structure du système immunitaire	true	Inferred relationship	Some	1
Lichtenstein syndrome	survenue (attribut)	congénital	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Id	Description	Lang	Type	Status	Case?	Module
3643231015	Lichtenstein syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3643232010	Lichtenstein syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
766301000241119	syndrome de Lichtenstein (trouble)	fr	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
975581000172116	syndrome de Lichtenstein	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3643233017	Syndrome with characteristics of frequent infections associated with osteoporosis, a tendency for fractures and osseous anomalies. It has been described in two monozygotic twin brothers. Transmission is autosomal recessive.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core