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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
1770548019 Lentiginosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
5260981000241119 lentiginose fr Synonym (core metadata concept) Active Entire term case insensitive (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

19 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lentiginosis Is a Disorder of skin colour false Inferred relationship Existential restriction modifier (core metadata concept)
Lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentiginosis Is a lentigo false Inferred relationship Existential restriction modifier (core metadata concept)
Lentiginosis Associated morphology Structure showing abnormal deposition of pigment (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentiginosis Associated morphology Increased melanin pigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentiginosis Associated morphology Increased melanin pigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentiginosis Finding site Structure of skin and/or mucous membrane (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentiginosis Is a Skin or mucosa lesion true Inferred relationship Existential restriction modifier (core metadata concept)
Lentiginosis Is a Hamartoma (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Lentiginosis Is a Disorder of body system false Inferred relationship Existential restriction modifier (core metadata concept)
Lentiginosis Is a Mass of body structure true Inferred relationship Existential restriction modifier (core metadata concept)
Lentiginosis Associated morphology Lentigo true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentiginosis Is a Melanosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital/hereditary lentiginosis Is a False Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Lentiginosis due to PUVA Is a True Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Mucosal lentiginosis Is a True Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Unilateral lentiginosis Is a False Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Genital lentiginosis Is a True Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Acquired lentiginosis Is a False Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Centrofacial lentiginosis syndrome Is a True Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Unilateral lentiginosis Associated finding False Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Unilateral lentiginosis Associated finding False Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Nevoid lentiginosis Is a False Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Labial lentigo Is a False Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Hypotrichosis with keratosis pilaris and lentiginosis Is a True Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Eruptive lentiginosis Is a True Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome Is a True Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
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 Inferred relationship Existential restriction modifier (core metadata concept)
syndrome de Moynahan Is a False Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Ocular albinism-lentigines-deafness syndrome Is a False Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Solar lentigo (disorder) Is a True Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Reticulate acropigmentation of Kitamura (disorder) Is a True Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Lentigo simplex (disorder) Is a True Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Solar lentiginosis Is a True Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome Is a True Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Zosteriform lentiginosis (disorder) Is a True Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
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 Inferred relationship Existential restriction modifier (core metadata concept)
Agminated lentiginosis (disorder) Is a True Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
Nevus spilus (disorder) Is a True Lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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