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402624000: Lentiginosis (disorder)

Status: current, 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
1770548019 Lentiginosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1781738015 Lentiginosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2020781000005110 Lentiginosis da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

19 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lentiginosis (disorder) Is a Disorder of skin color (disorder) false Inferred relationship Some
Lentiginosis (disorder) Finding site Skin structure false Inferred relationship Some 1
Lentiginosis (disorder) Is a Lentigo false Inferred relationship Some
Lentiginosis (disorder) Associated morphology Pigment deposition false Inferred relationship Some 1
Lentiginosis (disorder) Associated morphology øget melaninpigmentering false Inferred relationship Some 1
Lentiginosis (disorder) Finding site Skin structure false Inferred relationship Some 1
Lentiginosis (disorder) Associated morphology øget melaninpigmentering false Inferred relationship Some 1
Lentiginosis (disorder) Finding site Structure of skin and/or mucous membrane (body structure) true Inferred relationship Some 1
Lentiginosis (disorder) Is a Skin or mucosa lesion true Inferred relationship Some
Lentiginosis (disorder) Is a Hamartoma (disorder) true Inferred relationship Some
Lentiginosis (disorder) Is a Disorder of body system false Inferred relationship Some
Lentiginosis (disorder) Is a Mass of body structure true Inferred relationship Some
Lentiginosis (disorder) Associated morphology Lentigo (morphologic abnormality) true Inferred relationship Some 1
Lentiginosis (disorder) Is a Melanosis (disorder) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Kongenit/hereditær lentiginose Is a False Lentiginosis (disorder) Inferred relationship Some
Lentiginosis due to PUVA Is a True Lentiginosis (disorder) Inferred relationship Some
Mucosal lentiginosis Is a True Lentiginosis (disorder) Inferred relationship Some
Unilateral lentiginose Is a False Lentiginosis (disorder) Inferred relationship Some
Genital lentiginosis Is a True Lentiginosis (disorder) Inferred relationship Some
erhvervet lentiginose Is a False Lentiginosis (disorder) Inferred relationship Some
Centrofacial lentiginosis syndrome (disorder) Is a True Lentiginosis (disorder) Inferred relationship Some
Unilateral lentiginose Associated finding False Lentiginosis (disorder) Inferred relationship Some 1
Unilateral lentiginose Associated finding False Lentiginosis (disorder) Inferred relationship Some 1
Nevoid lentiginosis (disorder) Is a False Lentiginosis (disorder) Inferred relationship Some
Lentigo labialis Is a False Lentiginosis (disorder) Inferred relationship Some
Hypotrichosis with keratosis pilaris and lentiginosis (disorder) Is a True Lentiginosis (disorder) Inferred relationship Some
Eruptive lentiginosis Is a True Lentiginosis (disorder) Inferred relationship Some
Peutz-Jeghers syndrome Is a True Lentiginosis (disorder) Inferred relationship Some
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. Is a True Lentiginosis (disorder) Inferred relationship Some
Moynahans syndrom Is a False Lentiginosis (disorder) Inferred relationship Some
Okulær albinisme-lentigines-døvhedssyndrom Is a False Lentiginosis (disorder) Inferred relationship Some
Solar lentigo Is a True Lentiginosis (disorder) Inferred relationship Some
Reticulate acropigmentation of Kitamura Is a True Lentiginosis (disorder) Inferred relationship Some
Lentigo simplex (disorder) Is a True Lentiginosis (disorder) Inferred relationship Some
Solar lentiginosis (disorder) Is a True Lentiginosis (disorder) Inferred relationship Some
Multiple lentigines syndrome (disorder) Is a True Lentiginosis (disorder) Inferred relationship Some
Zosteriform lentiginosis (disorder) Is a True Lentiginosis (disorder) Inferred relationship Some
A rare association syndrome, reported in several members of two families to date, characterized by arterial dissection, occurring at an early age and presenting with a range of manifestations depending on the vascular territory involved (headache, dysphasia, hemiparesis), in association with cystic medial necrosis and multiple lentigines (brown and black in color and mainly affecting the skin of the trunk and extremities). Is a True Lentiginosis (disorder) Inferred relationship Some
Agminated lentiginosis (disorder) Is a True Lentiginosis (disorder) Inferred relationship Some
Nevus spilus (disorder) Is a True Lentiginosis (disorder) Inferred relationship Some

Reference Sets

Description inactivation indicator reference set

US English

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