2412005: Maculopapule (morphologic abnormality)

SNOMED CT Concept\Body structure (body structure)\Morphologically altered structure\Morphologically abnormal structure\Lesion (morphologic abnormality)\A small, solid lesion, less than 1 cm in diameter, raised above the surface of the surrounding skin and hence palpable\Maculopapule

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

5127013 Maculopapule en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

753721013 Maculopapule (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Maculopapule	Is a	A small, solid lesion, less than 1 cm in diameter, raised above the surface of the surrounding skin and hence palpable	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Late cutaneous pinta	Associated morphology	False	Maculopapule	Inferred relationship	Some	1
Cicatricial skin lesions of pinta	Associated morphology	False	Maculopapule	Inferred relationship	Some	3
Dyschromic skin lesions of pinta	Associated morphology	False	Maculopapule	Inferred relationship	Some	2
Achromic AND hyperchromic skin lesions of pinta	Associated morphology	False	Maculopapule	Inferred relationship	Some	2
Achromic skin lesions of pinta	Associated morphology	False	Maculopapule	Inferred relationship	Some	2
Mixed cutaneous pinta lesion	Associated morphology	False	Maculopapule	Inferred relationship	Some	1
Maculopapular rash	Is a	True	Maculopapule	Inferred relationship	Some
Maculopapular sarcoidosis	Associated morphology	True	Maculopapule	Inferred relationship	Some	3
A form of cutaneous mastocytosis (CM) characterised by the presence of multiple hyperpigmented macules, papules or nodules associated with abnormal accumulation of mast cells in the skin. Most patients present in infancy or childhood, but onset may also occur in adulthood. Mutations in the KIT gene (4q11-q12) have been identified however this mutation is rare in the paediatric population and the aetiology and pathogenesis in these cases remains to be determined. The disease generally occurs sporadically but rare familial cases have been reported.	Associated morphology	True	Maculopapule	Inferred relationship	Some	5
Telangiectasia macularis eruptiva perstans	Associated morphology	True	Maculopapule	Inferred relationship	Some	2

This concept is not in any reference sets