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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


12 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary hypermelanosis (disorder) est un(e) (attribut) hyperpigmentation de la peau true Inferred relationship Some
Hereditary hypermelanosis (disorder) localisation d'une constatation (attribut) Structure of skin region false Inferred relationship Some 1
Hereditary hypermelanosis (disorder) morphologie associée (attribut) Hyperpigmentation (morphologic abnormality) false Inferred relationship Some 2
Hereditary hypermelanosis (disorder) est un(e) (attribut) Melanosis (disorder) true Inferred relationship Some
Hereditary hypermelanosis (disorder) morphologie associée (attribut) mélanose (anomalie morphologique) true Inferred relationship Some 1
Hereditary hypermelanosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Hereditary hypermelanosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Hereditary hypermelanosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Hereditary hypermelanosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Hereditary hypermelanosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Hereditary hypermelanosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Hereditary hypermelanosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Hereditary hypermelanosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Hereditary hypermelanosis (disorder) localisation d'une constatation (attribut) structure de la peau true Inferred relationship Some 1
Hereditary hypermelanosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Hereditary hypermelanosis (disorder) est un(e) (attribut) Genetic disorder of skin pigmentation (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Centrofacial lentiginosis syndrome est un(e) (attribut) True Hereditary hypermelanosis (disorder) Inferred relationship Some
Acromelanosis est un(e) (attribut) True Hereditary hypermelanosis (disorder) Inferred relationship Some
Familial generalised lentiginosis est un(e) (attribut) True Hereditary hypermelanosis (disorder) Inferred relationship Some
Arterial dissection and lentiginosis syndrome (disorder) est un(e) (attribut) True Hereditary hypermelanosis (disorder) Inferred relationship Some
Hereditary benign acanthosis nigricans est un(e) (attribut) True Hereditary hypermelanosis (disorder) Inferred relationship Some
acanthosis nigricans héréditaire bénin avec insulinorésistance est un(e) (attribut) True Hereditary hypermelanosis (disorder) Inferred relationship Some
Hereditary lentiginosis (disorder) est un(e) (attribut) False Hereditary hypermelanosis (disorder) Inferred relationship Some
Hereditary diffuse melanosis (disorder) est un(e) (attribut) True Hereditary hypermelanosis (disorder) Inferred relationship Some
Hereditary reticulate melanosis (disorder) est un(e) (attribut) True Hereditary hypermelanosis (disorder) Inferred relationship Some
Genetic syndrome with hypermelanosis (disorder) est un(e) (attribut) True Hereditary hypermelanosis (disorder) Inferred relationship Some
Familial progressive hyperpigmentation (disorder) est un(e) (attribut) True Hereditary hypermelanosis (disorder) Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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