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765195000: Familial generalized lentiginosis (disorder)


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
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
5404505019 Familial generalized lentiginosis is a rare, inherited, skin hyperpigmentation disorder characterized by 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
5404506018 Familial generalised lentiginosis is a rare, inherited, skin hyperpigmentation disorder characterised by 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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial generalised lentiginosis Finding site Skin structure true Inferred relationship Some 1
Familial generalised lentiginosis Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Familial generalised lentiginosis Occurrence Congenital true Inferred relationship Some 1
Familial generalised lentiginosis Is a Lentiginosis (disorder) true Inferred relationship Some
Familial generalised lentiginosis Is a Genetic disorder of skin pigmentation (disorder) false Inferred relationship Some
Familial generalised lentiginosis Associated morphology Lentigo (morphologic abnormality) true Inferred relationship Some 1
Familial generalised lentiginosis Is a Congenital pigmentary skin anomalies true Inferred relationship Some
Familial generalised lentiginosis Is a Congenital hamartoma of skin (disorder) true Inferred relationship Some
Familial generalised lentiginosis Is a Congenital melanosis true Inferred relationship Some
Familial generalised lentiginosis Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Familial generalised lentiginosis Is a Hereditary hypermelanosis (disorder) true Inferred relationship Some
Familial generalised lentiginosis Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Arterial dissection and lentiginosis syndrome (disorder) Is a False Familial generalised lentiginosis Inferred relationship Some

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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