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403804008: 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
1793131000052117 ärftlig hypermelanos sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


12 descendants. Search Descendants:

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

Inbound Relationships Type Active Source Characteristic Refinability Group
ärftlig lentiginos 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 (disorder) Is a True Hereditary hypermelanosis (disorder) Inferred relationship Some
Centrofacial lentiginosis syndrome Is a True Hereditary hypermelanosis (disorder) Inferred relationship Some
Acromelanosis Is a True Hereditary hypermelanosis (disorder) Inferred relationship Some
Familial generalised lentiginosis Is a True Hereditary hypermelanosis (disorder) Inferred relationship Some
Arterial dissection and lentiginosis syndrome (disorder) 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

Reference Sets

Description inactivation indicator reference set

GB English

US English

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