403804008: Hereditary hypermelanosis (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Skin AND/OR mucosa finding (finding)\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Disorder of skin pigmentation (disorder)\Genetic disorder of skin pigmentation (disorder)\Hereditary hypermelanosis (disorder)
\Skin AND/OR mucosa finding (finding)\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Disorder of skin pigmentation (disorder)\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Genetic disorder of skin pigmentation (disorder)\Hereditary hypermelanosis (disorder)
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Skin deposits\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)

\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Genetic disorder of skin pigmentation (disorder)\Hereditary hypermelanosis (disorder)
\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)
\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Skin deposits\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)
\General finding of soft tissue\Disorder of soft tissue\Lesion of soft tissue (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Genetic disorder of skin pigmentation (disorder)\Hereditary hypermelanosis (disorder)
\General finding of soft tissue\Disorder of soft tissue\Lesion of soft tissue (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Genetic disorder of skin pigmentation (disorder)\Hereditary hypermelanosis (disorder)
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin deposits\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Hereditary hypermelanosis (disorder)
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Genetic disorder of skin pigmentation (disorder)\Hereditary hypermelanosis (disorder)
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin deposits\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Genetic disorder of skin pigmentation (disorder)\Hereditary hypermelanosis (disorder)
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Skin deposits\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)

\Disease\Genetic disease\Genetic disorder of skin pigmentation (disorder)\Hereditary hypermelanosis (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Hereditary hypermelanosis (disorder)
\Disease\Disorder of pigmentation (disorder)\Melanosis (disorder)\Hereditary hypermelanosis (disorder)
\Disease\Disorder of pigmentation (disorder)\Disorder of skin pigmentation (disorder)\Genetic disorder of skin pigmentation (disorder)\Hereditary hypermelanosis (disorder)
\Disease\Disorder of pigmentation (disorder)\Disorder of skin pigmentation (disorder)\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Hereditary hypermelanosis (disorder)
\Disease\Disorder of body system\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Disorder of skin pigmentation (disorder)\Genetic disorder of skin pigmentation (disorder)\Hereditary hypermelanosis (disorder)
\Disease\Disorder of body system\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Disorder of skin pigmentation (disorder)\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Hereditary hypermelanosis (disorder)
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Genetic disorder of skin pigmentation (disorder)\Hereditary hypermelanosis (disorder)
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin deposits\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)
\Disease\Disorder of soft tissue\Lesion of soft tissue (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Genetic disorder of skin pigmentation (disorder)\Hereditary hypermelanosis (disorder)
\Disease\Disorder of soft tissue\Lesion of soft tissue (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Genetic disorder of skin pigmentation (disorder)\Hereditary hypermelanosis (disorder)
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Disorder of skin pigmentation (disorder)\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin deposits\Hyperpigmentation of skin\Hereditary hypermelanosis (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

1771730019 Hereditary hypermelanosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1782813016 Hereditary hypermelanosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

6254381000241119 hypermélanose héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary hypermelanosis (disorder)	Is a	Hyperpigmentation of skin	true	Inferred relationship	Some
Hereditary hypermelanosis (disorder)	Finding site	Structure of skin region	false	Inferred relationship	Some	1
Hereditary hypermelanosis (disorder)	Associated morphology	Hyperpigmentation	false	Inferred relationship	Some	2
Hereditary hypermelanosis (disorder)	Is a	Melanosis (disorder)	true	Inferred relationship	Some
Hereditary hypermelanosis (disorder)	Associated morphology	Melanosis	true	Inferred relationship	Some	1
Hereditary hypermelanosis (disorder)	Finding site	Skin structure	false	Inferred relationship	Some	1
Hereditary hypermelanosis (disorder)	Finding site	Skin structure	false	Inferred relationship	Some	2
Hereditary hypermelanosis (disorder)	Finding site	Skin structure	false	Inferred relationship	Some	1
Hereditary hypermelanosis (disorder)	Finding site	Skin structure	false	Inferred relationship	Some	2
Hereditary hypermelanosis (disorder)	Finding site	Skin structure	false	Inferred relationship	Some	1
Hereditary hypermelanosis (disorder)	Finding site	Skin structure	false	Inferred relationship	Some	2
Hereditary hypermelanosis (disorder)	Finding site	Skin structure	false	Inferred relationship	Some	1
Hereditary hypermelanosis (disorder)	Finding site	Skin structure	false	Inferred relationship	Some	2
Hereditary hypermelanosis (disorder)	Finding site	Skin structure	true	Inferred relationship	Some	1
Hereditary hypermelanosis (disorder)	Finding site	Skin structure	false	Inferred relationship	Some	2
Hereditary hypermelanosis (disorder)	Is a	Genetic disorder of skin pigmentation (disorder)	true	Inferred relationship	Some
Hereditary hypermelanosis (disorder)	Is a	Hereditary disorder of the integument	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary lentiginosis	Is a	False	Hereditary hypermelanosis (disorder)	Inferred relationship	Some
Hereditary diffuse melanosis (disorder)	Is a	True	Hereditary hypermelanosis (disorder)	Inferred relationship	Some
Hereditary reticulate melanosis (disorder)	Is a	True	Hereditary hypermelanosis (disorder)	Inferred relationship	Some
Genetic syndrome with hypermelanosis (disorder)	Is a	True	Hereditary hypermelanosis (disorder)	Inferred relationship	Some
Familial progressive hyperpigmentation is a rare, genetic, skin pigmentation anomaly disorder characterized by irregular patches of hyperpigmented skin which present at birth or in early infancy and increase in size, number and confluence with age. Affected areas of the body include the face, neck, trunk and limbs, as well as the palms, soles, oral mucosa and conjunctiva. No hypopigmentation macules are observed and no systemic diseases are associated.	Is a	True	Hereditary hypermelanosis (disorder)	Inferred relationship	Some
Centrofacial lentiginosis syndrome	Is a	True	Hereditary hypermelanosis (disorder)	Inferred relationship	Some
Acromelanosis (disorder)	Is a	True	Hereditary hypermelanosis (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	Hereditary hypermelanosis (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	Hereditary hypermelanosis (disorder)	Inferred relationship	Some
Hereditary benign acanthosis nigricans	Is a	True	Hereditary hypermelanosis (disorder)	Inferred relationship	Some
Hereditary benign acanthosis nigricans with insulin resistance	Is a	True	Hereditary hypermelanosis (disorder)	Inferred relationship	Some
Hypermelanotic pigmentary mosaicism	Is a	True	Hereditary hypermelanosis (disorder)	Inferred relationship	Some

Reference Sets

Description inactivation indicator reference set

US English

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Id	Description	Lang	Type	Status	Case?	Module
1771730019	Hereditary hypermelanosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1782813016	Hereditary hypermelanosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6254381000241119	hypermélanose héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module