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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
1858621000195114 lentigginosi it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5260981000241119 lentiginose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

20 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 Increased melanin pigmentation false Inferred relationship Some 1
Lentiginosis (disorder) Finding site Skin structure false Inferred relationship Some 1
Lentiginosis (disorder) Associated morphology Increased melanin pigmentation 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
Congenital/hereditary lentiginosis 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 lentiginosis Is a False Lentiginosis (disorder) Inferred relationship Some
Genital lentiginosis Is a True Lentiginosis (disorder) Inferred relationship Some
Acquired lentiginosis Is a False Lentiginosis (disorder) Inferred relationship Some
Centrofacial lentiginosis syndrome Is a True Lentiginosis (disorder) Inferred relationship Some
Unilateral lentiginosis Associated finding False Lentiginosis (disorder) Inferred relationship Some 1
Unilateral lentiginosis Associated finding False Lentiginosis (disorder) Inferred relationship Some 1
Nevoid lentiginosis (disorder) Is a False Lentiginosis (disorder) Inferred relationship Some
Labial lentigo Is a False Lentiginosis (disorder) Inferred relationship Some
Hypotrichosis with keratosis pilaris and lentiginosis 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
syndrome de Moynahan Is a False Lentiginosis (disorder) Inferred relationship Some
Ocular albinism-lentigines-deafness syndrome 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 Is a True Lentiginosis (disorder) Inferred relationship Some
Multiple lentigines syndrome 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

GB English

US English

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