765195000: lentiginose généralisée familiale (trouble)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

1001781000172114 syndrome des lentigines multiples familial sans manifestation systémique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

3657404011 Familial generalised lentiginosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3657405012 Familial generalized lentiginosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3657406013 Familial generalized lentiginosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3657407016 Familial multiple lentigines syndrome without systemic involvement en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3657408014 Familial lentigines profusa en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

767671000241116 lentiginose généralisée familiale (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

908251000172110 lentiginose généralisée familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

3657285012 A rare inherited skin hyperpigmentation disorder with characteristics of widespread lentigines without associated noncutaneous abnormalities. Patients present multiple brown to dark brown, non-elevated macula of 0.2 to 1 cm in diameter, spread over the entire body, sometimes including palms or soles, but never oral mucosa. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial generalised lentiginosis	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Familial generalised lentiginosis	est un(e) (attribut)	Hereditary hypermelanosis (disorder)	true	Inferred relationship	Some
Familial generalised lentiginosis	est un(e) (attribut)	Developmental hereditary disorder	true	Inferred relationship	Some
Familial generalised lentiginosis	localisation d'une constatation (attribut)	structure de la peau	true	Inferred relationship	Some	1
Familial generalised lentiginosis	est un(e) (attribut)	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Familial generalised lentiginosis	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Familial generalised lentiginosis	est un(e) (attribut)	Lentiginosis (disorder)	true	Inferred relationship	Some
Familial generalised lentiginosis	est un(e) (attribut)	Genetic disorder of skin pigmentation (disorder)	false	Inferred relationship	Some
Familial generalised lentiginosis	morphologie associée (attribut)	Lentigo (morphologic abnormality)	true	Inferred relationship	Some	1
Familial generalised lentiginosis	est un(e) (attribut)	anomalies congénitales de pigmentation de la peau	true	Inferred relationship	Some
Familial generalised lentiginosis	est un(e) (attribut)	Congenital hamartoma of skin (disorder)	true	Inferred relationship	Some
Familial generalised lentiginosis	est un(e) (attribut)	Congenital melanosis (disorder)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Arterial dissection and lentiginosis syndrome (disorder)	est un(e) (attribut)	False	Familial generalised lentiginosis	Inferred relationship	Some

Reference Sets

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

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1001781000172114	syndrome des lentigines multiples familial sans manifestation systémique	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3657404011	Familial generalised lentiginosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3657405012	Familial generalized lentiginosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3657406013	Familial generalized lentiginosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3657407016	Familial multiple lentigines syndrome without systemic involvement	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3657408014	Familial lentigines profusa	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
767671000241116	lentiginose généralisée familiale (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
908251000172110	lentiginose généralisée familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3657285012	A rare inherited skin hyperpigmentation disorder with characteristics of widespread lentigines without associated noncutaneous abnormalities. Patients present multiple brown to dark brown, non-elevated macula of 0.2 to 1 cm in diameter, spread over the entire body, sometimes including palms or soles, but never oral mucosa.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core