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767376003: Lentigo (morphologic abnormality)

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
3670916013 Lentigo (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3670917016 Lentigo en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3670916013 Lentigo (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3670917016 Lentigo en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lentigo Is a Hamartoma true Inferred relationship Existential restriction modifier (core metadata concept)
Lentigo Is a Melanosis true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Labial lentigo Associated morphology False Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 2
Labial lentigo Associated morphology False Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypotrichosis with keratosis pilaris and lentiginosis Associated morphology False Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentiginosis Associated morphology True Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
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. Associated morphology True Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Peutz-Jeghers polyps of small bowel Associated morphology False Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 2
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). Associated morphology False Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 2
Nevoid lentiginosis Associated morphology False Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 2
syndrome de Moynahan Associated morphology False Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Ocular albinism-lentigines-deafness syndrome Associated morphology False Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 2
Solar lentigo (disorder) Associated morphology False Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Reticulate acropigmentation of Kitamura (disorder) Associated morphology True Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 2
Lentigo simplex (disorder) Associated morphology False Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Mucosal lentiginosis Associated morphology True Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Genital lentiginosis Associated morphology True Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Solar lentiginosis Associated morphology True Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Centrofacial lentiginosis syndrome Associated morphology True Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple lentigines syndrome Associated morphology True Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 2
Multiple lentigines syndrome Associated morphology False Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentiginosis due to PUVA Associated morphology True Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Zosteriform lentiginosis (disorder) Associated morphology True Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Peutz-Jeghers syndrome Associated morphology False Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Peutz-Jeghers polyps of small bowel Associated morphology True Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 3
Eruptive lentiginosis Associated morphology False Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
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). Associated morphology True Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple lentigines syndrome Associated morphology False Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 3
Lentiginous melanocytic nevus Is a True Lentigo Inferred relationship Existential restriction modifier (core metadata concept)
Eruptive lentigo Is a True Lentigo Inferred relationship Existential restriction modifier (core metadata concept)
Lentigo of lip (disorder) Associated morphology True Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Agminated lentiginosis (disorder) Associated morphology True Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 1
Peutz-Jeghers syndrome Associated morphology True Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypotrichosis with keratosis pilaris and lentiginosis Associated morphology True Lentigo Inferred relationship Existential restriction modifier (core metadata concept) 2
Solar lentigo (morphologic abnormality) Is a True Lentigo Inferred relationship Existential restriction modifier (core metadata concept)
Simple lentigo Is a True Lentigo Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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